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@article{MBB_2019_14_1_a4, author = {Ya. R. Efremov and A. S. Proskurina and E. A. Potter and E. V. Dolgova and O. V. Efremova and D. Yu. Oshchepkov and N. A. Kolchanov and S. S. Bogachev}, title = {Cancer stem cells: {``Emergency} service'' for tumors under generalized cellular stress}, journal = {Matemati\v{c}eska\^a biologi\^a i bioinformatika}, pages = {306--326}, publisher = {mathdoc}, volume = {14}, number = {1}, year = {2019}, language = {ru}, url = {http://geodesic.mathdoc.fr/item/MBB_2019_14_1_a4/} }
TY - JOUR AU - Ya. R. Efremov AU - A. S. Proskurina AU - E. A. Potter AU - E. V. Dolgova AU - O. V. Efremova AU - D. Yu. Oshchepkov AU - N. A. Kolchanov AU - S. S. Bogachev TI - Cancer stem cells: ``Emergency service'' for tumors under generalized cellular stress JO - Matematičeskaâ biologiâ i bioinformatika PY - 2019 SP - 306 EP - 326 VL - 14 IS - 1 PB - mathdoc UR - http://geodesic.mathdoc.fr/item/MBB_2019_14_1_a4/ LA - ru ID - MBB_2019_14_1_a4 ER -
%0 Journal Article %A Ya. R. Efremov %A A. S. Proskurina %A E. A. Potter %A E. V. Dolgova %A O. V. Efremova %A D. Yu. Oshchepkov %A N. A. Kolchanov %A S. S. Bogachev %T Cancer stem cells: ``Emergency service'' for tumors under generalized cellular stress %J Matematičeskaâ biologiâ i bioinformatika %D 2019 %P 306-326 %V 14 %N 1 %I mathdoc %U http://geodesic.mathdoc.fr/item/MBB_2019_14_1_a4/ %G ru %F MBB_2019_14_1_a4
Ya. R. Efremov; A. S. Proskurina; E. A. Potter; E. V. Dolgova; O. V. Efremova; D. Yu. Oshchepkov; N. A. Kolchanov; S. S. Bogachev. Cancer stem cells: ``Emergency service'' for tumors under generalized cellular stress. Matematičeskaâ biologiâ i bioinformatika, Tome 14 (2019) no. 1, pp. 306-326. http://geodesic.mathdoc.fr/item/MBB_2019_14_1_a4/
[1] P. J. Fialkow, G. Klein, S. M. Gartler, P. Clifford, “Clonal origin for individual Burkitt tumours”, The Lancet, 1 (1970), 384–386 | DOI
[2] P. J. Fialkow, S. M. Gartler, A. Yoshida, “Clonal origin of chronic myelocytic leukemia in man”, Proc. Natl. Acad. Sci. USA, 58 (1967), 1468–1471 | DOI
[3] M. W. Steele, “Clonal origin for individual Burkitt tumours”, Lancet, 1 (1970), 677 | DOI
[4] S. B. Baylin, D. S. Gann, S. H. Hsu, “Clonal origin of inherited medullary thyroid carcinoma and pheochromocytoma”, Science, 193 (1976), 321–323 | DOI
[5] P. C. Nowell, “The clonal evolution of tumor cell populations”, Science, 194 (1976), 23–28 | DOI
[6] G. Mendez, R. Quencer, M. Post, N. Stokes, “Malignant external otitis: a radiographic-clinical correlation”, Am. J. Roentgenol, 132 (1979), 957–961 | DOI
[7] V. A. Lavrovsky, M. A. Guvakova, Y. V. Lavrovsky, “High frequency of tumour cell reversion to non-tumorigenic phenotype”, Eur. J. Cancer, 28 (1992), 17–21 | DOI
[8] S. Pathak, “Cytogenetic abnormalities in cancer: with special emphasis on tumor heterogeneity”, Cancer Metastasis Rev, 8 (1990), 299–318 | DOI
[9] D. E. Mattox, D. D. Von Hoff, “Culture of human head and neck cancer stem cells using soft agar”, Arch. Otolaryngol, 106 (1980), 672–674 | DOI
[10] T. Reya, S. J. Morrison, M. F. Clarke, I. L. Weissman, “Stem cells, cancer, cancer stem cells”, Nature, 414 (2001), 105–111 | DOI
[11] R. Schofield, “The relationship between the spleen colony-forming cell and the haemopoietic stem cell”, Blood Cells, 4 (1978), 7–25
[12] R. Schofield, “The stem cell system”, Biomed. Pharmacother, 37 (1983), 375–380
[13] H. Lin, “The stem-cell niche theory: lessons from flies”, Nat. Rev. Genet., 3 (2002), 931–940 | DOI
[14] V. Marthiens, I. Kazanis, L. Moss, K. Long, C. Ffrench-Constant, Adhesion molecules in the stem cell niche – more than just staying in shape?, J. Cell Sci., 123 (2010), 1613–1622 | DOI
[15] J. Voog, D. L. Jones, “Stem cells and the niche: A dynamic duo”, Cell Stem Cell, 6 (2010), 103–115 | DOI
[16] L. E. O'Brien, D. Bilder, “Beyond the niche: tissue-level coordination of stem cell dynamics”, Annu. Rev. Cell Dev. Biol., 29 (2013), 107–136 | DOI
[17] E. V. Dolgova, E. A. Alyamkina, Y. R. Efremov, V. P. Nikolin, N. A. Popova, T. V. Tyrinova, A. V. Kozel, A. M. Minkevich, O. M. Andrushkevich, E. L. Zavyalov et al, “Identification of cancer stem cells and a strategy for their elimination”, Cancer Biol. Ther., 15 (2014), 1378–1394 | DOI
[18] E. A. Potter, E. V. Dolgova, A. S. Proskurina, A. M. Minkevich, Y. R. Efremov, O. S. Taranov, V. V. Omigov, V. P. Nikolin, N. A. Popova, S. I. Bayborodin et al, “A strategy to eradicate well-developed Krebs-2 ascites in mice”, Oncotarget, 7 (2016), 11580–11594 | DOI
[19] E. A. Potter, E. V. Dolgova, A. S. Proskurina, Y. R. Efremov, O. S. Taranov, V. P. Nikolin, N. A. Popova, T. D. Dubatolova, D. D. Petrova, E. I. Vereschagin et al, “Development of the therapeutic regimen based on the synergistic activity of cyclophosphamide and doublestranded DNA preparation which results in complete cure of mice engrafted with Krebs-2 ascites”, Vavilov J. Genet. Breed, 20 (2016), 723–735 | DOI
[20] R. G. Greig, T. P. Koestler, D. L. Trainer, S. P. Corwin, L. Miles, T. Kline, R. Sweet, S. Yokoyama, G. Poste, “Tumorigenic and metastatic properties of “normal” and ras-transfected NIH/3T3 cells”, Proc. Natl. Acad. Sci. USA, 82 (1985), 3698–3701 | DOI
[21] A. Melchiori, A. Colacci, P. L. Lollini, C. De Giovanni, S. Carlone, S. Grilli, S. Parodi, A. Albini, “Induction of invasive and experimental metastasis potential in BALB/c 3T3 cells by benzo(a)pyrene transformation”, Invasion Metastasis, 12 (1992), 1–11
[22] A. Tuccitto, M. Tazzari, V. Beretta, F. Rini, C. Miranda, A. Greco, M. Santinami, R. Patuzzo, B. Vergani, A. Villa et al, “Immunomodulatory factors control the fate of melanoma tumor initiating cells”, Stem Cells, 34 (2016), 2449–2460 | DOI
[23] W. M. ElShamy, R. J. Duhé, “Overview: Cellular plasticity, cancer stem cells and metastasis”, Cancer Lett, 341 (2013), 2–8 | DOI
[24] E. Campos-Sánchez, C. Cobaleda, “Tumoral reprogramming: Plasticity takes a walk on the wild side”, Biochim. Biophys. Acta, 1849 (2015), 436–447 | DOI
[25] E. Potter, E. Dolgova, A. Proskurina, Y. Efremov, A. Minkevich, A. Rozanov, S. Peltek, V. Nikolin, N. Popova, I. Seledtsov et al, “Gene expression profiling of tumor-initiating stem cells from mouse Krebs-2 carcinoma using a novel marker of poorly differentiated cells”, Oncotarget, 8 (2017), 9425–9441 | DOI
[26] Ya. R. Efremov, A. S. Proskurina, E. A. Potter, E. V. Dolgova, O. V. Efremova, S. S. Bogachev, “In i yan plyuripotentnosti: rezultaty analiza genov, demonstriruyuschikh povyshennuyu ekspressiyu v initsiiruyuschikh opukholevykh kletkakh astsitnoi kartsinomy Krebs-2”, Matematicheskaya biologiya i bioinformatika, 14:1 (2019), 160–187
[27] J. A. Bertout, S. A. Patel, M. C. Simon, “The impact of O2 availability on human cancer”, Nat. Rev. Cancer, 8 (2008), 967–975 | DOI
[28] J. E. Moulder, S. Rockwell, “Tumor hypoxia: its impact on cancer therapy”, Cancer Metastasis Rev, 5 (1987), 313–341 | DOI
[29] C. Murr, L. C. Fuith, B. Widner, B. Wirleitner, G. Baier-Bitterlich, D. Fuchs, Increased neopterin concentrations in patients with cancer: Indicator of oxidative stress?, Anticancer Res, 19 (1999), 1721–1728
[30] A. Laviano, M. M. Meguid, I. Preziosa, F. R. Fanelli, “Oxidative stress, wasting in cancer”, Curr. Opin. Clin. Nutr. Metab. Care, 10 (2007), 449–456 | DOI
[31] K. Kurz, S. Schroecksnadel, G. Weiss, D. Fuchs, “Association between increased tryptophan degradation and depression in cancer patients”, Curr. Opin. Clin. Nutr. Metab. Care, 14 (2011), 49–56 | DOI
[32] M. S. Poormasjedi-Meibod, S. Salimi Elizei, V. Leung, R. Baradar Jalili, F. Ko, A. Ghahary, “Kynurenine modulates MMP-1 and type-I collagen expression via aryl hydrocarbon receptor activation in dermal fibroblasts”, J. Cell. Physiol, 231 (2016), 2749–2760 | DOI
[33] A. A. Hammoud, N. Kirstein, V. Mournetas, A. Darracq, S. Broc, C. Blanchard, D. Zeineddine, M. Mortada, H. Boeuf, “Murine embryonic stem cell plasticity is regulated through klf5 and maintained by metalloproteinase mmp1 and hypoxia”, PLoS One, 11 (2016), e0146281 | DOI
[34] P. López-Iglesias, Y. Alcaina, N. Tapia, D. Sabour, M. J. Arauzo-Bravo, D. Sainz de la Maza, E. Berra, A. N. O'Mara, M. Nistal, S. Ortega et al, “Hypoxia induces pluripotency in primordial germ cells by HIF1$\alpha$ stabilization and Oct4 deregulation”, Antioxid. Redox Signal, 22 (2015), 205–223 | DOI
[35] A. Mohyeldin, T. Garzón-Muvdi, A. Quiñones-Hinojosa, “Oxygen in stem cell biology: A critical component of the stem cell niche”, Cell Stem Cell, 7 (2010), 150–161 | DOI
[36] K. M. Bae, Y. Dai, J. Vieweg, D. W. Siemann, “Hypoxia regulates SOX2 expression to promote prostate cancer cell invasion and sphere formation”, Am. J. Cancer Res, 6 (2016), 1078–1088
[37] E. J. Seo, D. K. Kim, I. H. Jang, E. J. Choi, S. H. Shin, S. I. Lee, S. M. Kwon, K. H. Kim, D. S. Suh, J. H. Kim, “Hypoxia-NOTCH1-SOX2 signaling is important for maintaining cancer stem cells in ovarian cancer”, Oncotarget, 7 (2016), 55624–55638 | DOI
[38] H. Iida, M. Suzuki, R. Goitsuka, H. Ueno, “Hypoxia induces CD133 expression in human lung cancer cells by up-regulation of OCT3/4 and SOX2”, Int. J. Oncol, 40 (2012), 71–79
[39] Z. Li, J. N. Rich, “Hypoxia and hypoxia inducible factors in cancer stem cell maintenance”, Current Topics in Microbiology and Immunology, 2010, 21–30
[40] T. Plösch, A. Gellhaus, E. M.E. Van Straten, N. Wolf, N. C.A. Huijkman, M. Schmidt, C. E. Dunk, F. Kuipers, E. Winterhager, The liver X receptor (LXR) and its target gene ABCA1 are regulated upon low oxygen in human trophoblast cells: A reason for alterations in preeclampsia?, Placenta, 31 (2010), 910–918 | DOI
[41] T. Liu, X. Wang, Y. Bai, H. Liao, S. Qiu, Y. Yang, X. Yan, J. Chen, H. Guo, S. Zhang, “The HIF-2alpha dependent induction of PAP and adenosine synthesis regulates glioblastoma stem cell function through the A2B adenosine receptor”, Int. J. Biochem. Cell Biol, 49 (2014), 8–16 | DOI
[42] R. B. Hough, J. Piatigorsky, “Preferential transcription of rabbit Aldh1a1 in the cornea: implication of hypoxia-related pathways”, Mol. Cell. Biol, 24 (2004), 1324–1340 | DOI
[43] A. Lundqvist, M. Sandstedt, J. Sandstedt, R. Wickelgren, G. I. Hansson, A. Jeppsson, L. M. Hultén, “The arachidonate 15-lipoxygenase enzyme product 15-HETE is present in heart tissue from patients with ischemic heart disease and enhances clot formation”, PLoS One, 11 (2016), e0161629 | DOI
[44] I. Jam, M. Shoham, R. O. Wolf, S. Mishkin, “Elevated serum amylase activity in the absence of clinical pancreatic or salivary gland disease: possible role of acute hypoxemia”, Am. J. Gastroenterol, 70 (1978), 480–488
[45] B. Chen, J. Xue, X. Meng, J. L. Slutzky, A. E. Calvert, L. G. Chicoine, “Resveratrol prevents hypoxia-induced arginase II expression and proliferation of human pulmonary artery smooth muscle cells via Akt-dependent signaling”, Am. J. Physiol. Cell. Mol. Physiol., 307 (2014), L317–L325 | DOI
[46] W. Han, T. Takano, J. He, J. Ding, S. Gao, C. Noda, S. Yanagi, H. Yamamura, “Role of BLNK in oxidative stress signaling in B cells”, Antioxidants Redox Signal, 3 (2001), 1065–1073 | DOI
[47] R. Li, Y. Wang, Z. Yang, Y. He, T. Zhao, M. Fan, X. Wang, L. Zhu, X. Wang, “Hypoxia-inducible factor-1$\alpha$ regulates the expression of L-type voltage-dependent Ca(2+) channels in PC12 cells under hypoxia”, Cell Stress Chaperones, 20 (2015), 507–516 | DOI
[48] A. Ricciardi, A. R. Elia, P. Cappello, M. Puppo, C. Vanni, P. Fardin, A. Eva, D. Munroe, X. Wu, M. Giovarelli, L. Varesio, “Transcriptome of hypoxic immature dendritic cells: Modulation of chemokine/receptor expression”, Mol. Cancer Res, 6 (2008), 175–185 | DOI
[49] L. Botto, E. Beretta, A. Bulbarelli, I. Rivolta, B. Lettiero, B. E. Leone, G. Miserocchi, P. Palestini, B. Lettiero, L. Barbara et al, “Hypoxia-induced modifications in plasma membranes and lipid microdomains in A549 cells and primary human alveolar cells”, J. Cell. Biochem, 105 (2008), 503–513 | DOI
[50] R. C. Brown, K. S. Mark, R. D. Egleton, J. D. Huber, A. R. Burroughs, T. P. Davis, “Protection against hypoxia-induced increase in blood-brain barrier permeability: role of tight junction proteins and NFkappaB”, J. Cell Sci., 116 (2003), 693–700 | DOI
[51] F. Martin, T. Linden, D. M. Katschinski, F. Oehme, I. Flamme, C. K. Mukhopadhyay, K. Eckhardt, J. Tr-ger, S. Barth, G. Camenisch, R. H. Wenger, “Copper-dependent activation of hypoxia-inducible factor (HIF)-1: implications for ceruloplasmin regulation”, Blood, 105 (2005), 4613–4619 | DOI
[52] Y. Ganat, S. Soni, M. Chacon, M. L. Schwartz, F. M. Vaccarino, “Chronic hypoxia up-regulates fibroblast growth factor ligands in the perinatal brain and induces fibroblast growth factor-responsive radial glial cells in the sub-ependymal zone”, Neuroscience, 112 (2002), 977–991 | DOI
[53] J. F. Mouillet, R. B. Donker, T. Mishima, T. Cronqvist, T. Chu, Y. Sadovsky, “The unique expression and function of miR-424 in human placental trophoblasts1”, Biol. Reprod, 89 (2013), 25 | DOI
[54] A. Mishra, J. Wang, Y. Shiozawa, S. McGee, J. Kim, Y. Jung, J. Joseph, J. E. Berry, A. Havens, K. J. Pienta, R. S. Taichman, “Hypoxia stabilizes GAS6/Axl signaling in metastatic prostate cancer”, Mol. Cancer Res, 10 (2012), 703–712 | DOI
[55] K. Y. Hsiao, M. H. Wu, N. Chang, S. H. Yang, C. W. Wu, H. S. Sun, S. J. Tsai, “Coordination of AUF1 and miR-148a destabilizes DNA methyltransferase 1 mRNA under hypoxia in endometriosis”, Mol. Hum. Reprod, 21 (2015), 894–904 | DOI
[56] X. Li, Y. Yang, J. Fang, H. Zhang, “FIZZ1 could enhance the angiogenic ability of rat aortic endothelial cells”, Int. J. Clin. Exp. Pathol, 6 (2013), 1847–1853
[57] Q. Yang, M. Sun, R. Ramchandran, J. U. Raj, “IGF-1 signaling in neonatal hypoxia-induced pulmonary hypertension: Role of epigenetic regulation”, Vascul. Pharmacol, 73 (2015), 20–31 | DOI
[58] “A. Jögi, J. Vallon-Christersson, L. Holmquist, H. Axelson, Å. Borg, S. Påhlman”, Human neuroblastoma cells exposed to hypoxia: induction of genes associated with growth, survival, and aggressive behavior, 295 (2004), 469–487
[59] L. Xu, X. Wang, J. Wang, D. Liu, Y. Wang, Z. Huang, H. Tan, “Hypoxia-induced secretion of IL-10 from adipose-derived mesenchymal stem cell promotes growth and cancer stem cell properties of Burkitt lymphoma”, Tumor Biol, 37 (2016), 7835–7842 | DOI
[60] N. Chaudary, M. Milosevic, R. P. Hill, “Suppression of vascular endothelial growth factor receptor 3 (VEGFR3) and vascular endothelial growth factor C (VEGFC) inhibits hypoxia-induced lymph node metastases in cervix cancer”, Gynecol. Oncol, 123 (2011), 393–400 | DOI | MR
[61] M. Slevin, J. Krupinski, N. Rovira, M. Turu, A. Luque, M. Baldellou, C. Sanfeliu, N. de Vera, L. Badimon, “Identification of pro-angiogenic markers in blood vessels from stroked-affected brain tissue using laser-capture microdissection”, BMC Genomics, 10 (2009), 113 | DOI
[62] P. Wang, J. Xu, Z. Hou, F. Wang, Y. Song, J. Wang, H. Zhu, H. Jin, “miRNA-34a promotes proliferation of human pulmonary artery smooth muscle cells by targeting PDGFRA”, Cell Prolif, 49 (2016), 484–493 | DOI
[63] S. Fu, K. P. Davies, “Opiorphin-dependent upregulation of CD73 (a key enzyme in the adenosine signaling pathway) in corporal smooth muscle cells exposed to hypoxic conditions and in corporal tissue in pre-priapic sickle cell mice”, Int. J. Impot. Res, 27 (2015), 140–145 | DOI
[64] D. Shen, Y. Wang, “Changes of plasma level of neurotensin, somatostatin, and dynorphin A in pilots under acute hypoxia”, Mil. Med, 163 (1998), 120–121 | DOI
[65] S. S. Pullamsetti, G. A. Banat, A. Schmall, M. Szibor, D. Pomagruk, J. Hänze, E. Kolosionek, J. Wilhelm, T. Braun, F. Grimminger et al, “Phosphodiesterase-4 promotes proliferation and angiogenesis of lung cancer by crosstalk with HIF”, Oncogene, 32 (2013), 1121–1134 | DOI
[66] R. Van Thienen, E. Masschelein, G. D'Hulst, M. Thomis, P. Hespel, “Twin resemblance in muscle HIF-1$\alpha$ responses to hypoxia and exercise”, Front. Physiol, 7 (2017), 676
[67] C. B. Peek, D. C. Levine, J. Cedernaes, A. Taguchi, Y. Kobayashi, S. J. Tsai, N. A. Bonar, M. R. McNulty, K. M. Ramsey, J. Bass, “Circadian clock interaction with HIF1$\alpha$ mediates oxygenic metabolism and anaerobic glycolysis in skeletal muscle”, Cell Metab, 25 (2017), 86–92 | DOI
[68] D. Shen, Y. Wang, “Effects of hypoxia on platelet activation in pilots”, Aviat. Space. Environ. Med, 65 (1994), 646–648
[69] J. LeCouter, R. Lin, M. Tejada, G. Frantz, F. Peale, K. J. Hillan, N. Ferrara, “The endocrine-gland-derived VEGF homologue Bv8 promotes angiogenesis in the testis: Localization of Bv8 receptors to endothelial cells”, Proc. Natl. Acad. Sci, 100 (2003), 2685–2690 | DOI
[70] G. K. Friedman, M. C. Haas, V. M. Kelly, J. M. Markert, G. Y. Gillespie, K. A. Cassady, “Hypoxia moderates $\gamma$134.5-deleted herpes simplex virus oncolytic activity in human glioma xenoline primary cultures”, Transl. Oncol, 5 (2012), 200–207 | DOI
[71] C. Royer, J. Lachuer, G. Crouzoulon, J. Roux, J. Peyronnet, J. Mamet, J. Pequignot, Y. Dalmaz, “Effects of gestational hypoxia on mRNA levels of Glut3 and Glut4 transporters, hypoxia inducible factor-1 and thyroid hormone receptors in developing rat brain”, Brain Res, 856 (2000), 119–128 | DOI
[72] M. A. Applebaum, A. R. Jha, C. Kao, K. M. Hernandez, G. DeWane, H. R. Salwen, A. Chlenski, M. Dobratic, C. J. Mariani, L. A. Godley et al, “Integrative genomics reveals hypoxia inducible genes that are associated with a poor prognosis in neuroblastoma patients”, Oncotarget, 7 (2016), 76816–76826 | DOI
[73] Q. F. Wu, C. Qian, N. Zhao, Q. Dong, J. Li, B. B. Wang, L. Chen, L. Yu, B. Han, Y. M. Du, Y. H. Liao, “Activation of transient receptor potential vanilloid 4 involves in hypoxia/reoxygenation injury in cardiomyocytes”, Cell Death Dis., 8 (2017), e2828 | DOI
[74] L. Chen, T. Fink, P. Ebbesen, V. Zachar, “Temporal transcriptome of mouse ATDC5 chondroprogenitors differentiating under hypoxic conditions”, Exp. Cell Res, 312 (2006), 1727–1744 | DOI
[75] Y. Ma, W. Yu, A. Shrivastava, F. Alemi, K. Lankachandra, R. K. Srivastava, S. Shankar, “Sanguinarine inhibits pancreatic cancer stem cell characteristics by inducing oxidative stress and suppressing sonic hedgehog-Gli-Nanog pathway”, Carcinogenesis, 38 (2017), 1047–1056 | DOI
[76] A. Cipak, L. Mrakovcic, M. Ciz, A. Lojek, B. Mihaylova, I. Goshev, M. Jaganjac, M. Cindric, S. Sitic, M. Margaritoni et al, “Growth suppression of human breast carcinoma stem cells by lipid peroxidation product 4-hydroxy-2-nonenal and hydroxyl radical-modified collagen”, Acta Biochim. Pol, 57 (2010), 165–171
[77] H. Saijo, Y. Hirohashi, T. Torigoe, R. Horibe, A. Takaya, A. Murai, T. Kubo, T. Kajiwara, T. Tanaka, Y. Shionoya et al, “Plasticity of lung cancer stem-like cells is regulated by the transcription factor HOXA5 that is induced by oxidative stress”, Oncotarget, 7 (2016), 50043–50056 | DOI
[78] K. Gopal, N. Gupta, H. Zhang, A. Alshareef, H. Alqahtani, G. Bigras, J. Lewis, D. Douglas, N. Kneteman, A. Lavasanifar, R. Lai, “Oxidative stress induces the acquisition of cancer stem-like phenotype in breast cancer detectable by using a Sox2 regulatory region-2 (SRR2) reporter”, Oncotarget, 7 (2016), 3111–3127 | DOI
[79] A. A. Dayem, H. Y. Choi, J. H. Kim, S. G. Cho, “Role of oxidative stress in stem, cancer, and cancer stem cells”, Cancers (Basel), 2 (2010), 859–884 | DOI
[80] N. A. Davies, L. Watkeys, L. Butcher, S. Potter, M. G. Hughes, H. Moir, K. Morris, A. W. Thomas, R. Webb, “The contributions of oxidative stress, oxidised lipoproteins and AMPK towards exercise-associated PPAR$\gamma$ signalling within human monocytic cells”, Free Radic. Res, 49 (2015), 45–56 | DOI
[81] A. W. Obianime, I. I. Roberts, “Antioxidants, cadmium-induced toxicity, serum biochemical and the histological abnormalities of the kidney and testes of the male Wistar rats”, Niger. J. Physiol. Sci, 24 (2009), 177–185
[82] B. Strzalka-Mrozik, L. Prudlo, M. W. Kimsa, M. C. Kimsa, M. Kapral, M. Nita, U. Mazurek, “Quantitative analysis of SOD2, ALDH1A1 and MGST1 messenger ribonucleic acid in anterior lens epithelium of patients with pseudoexfoliation syndrome”, Mol. Vis, 19 (2013), 1341–1349
[83] J. E. Jung, H. Karatas, Y. Liu, A. Yalcin, J. Montaner, E. H. Lo, K. Van Leyen, “STAT-dependent upregulation of 12/15-lipoxygenase contributes to neuronal injury after stroke”, J. Cereb. Blood Flow Metab, 35 (2015), 2043–2051 | DOI
[84] R. M. Touyz, “Linking LOX-1 and arginase II through mitochondria: A novel paradigm in endothelial dysfunction”, Circ. Res., 115 (2014), 412–414 | DOI
[85] L. Michalec, B. K. Choudhury, E. Postlethwait, J. S. Wild, R. Alam, M. Lett-Brown, S. Sur, “CCL7 and CXCL10 orchestrate oxidative stress-induced neutrophilic lung inflammation”, J. Immunol., 168 (2002), 846–852 | DOI
[86] S. Gupta, T. S. Silva, J. E. Osizugbo, L. Tucker, H. M. Spratt, N. J. Garg, “Serum-mediated activation of macrophages reflects TcVac2 vaccine efficacy against chagas disease”, Infect. Immun, 82 (2014), 1382–1389 | DOI
[87] A. Iborra, M. Mayorga, N. Llobet, P. Martínez, “Expression of complement regulatory proteins [membrane cofactor protein (CD46), decay accelerating factor (CD55), and protectin (CD59)] in endometrial stressed cells”, Cell. Immunol, 223 (2003), 46–51 | DOI
[88] C. Luna, G. Li, J. Qiu, D. L. Epstein, P. Gonzalez, “Role of miR-29b on the regulation of the extracellular matrix in human trabecular meshwork cells under chronic oxidative stress”, Mol. Vis, 15 (2009), 2488–2497
[89] M. G. F. Wahba, B. A.S. Messiha, A. A. Abo-Saif, “Protective effects of fenofibrate and resveratrol in an aggressive model of rheumatoid arthritis in rats”, Pharm. Biol, 54 (2016), 1705–1715 | DOI
[90] F. S. Dzugkoeva, I. V. Mozhaeva, S. G. Dzugkoev, O. I. Margieva, A. I. Tedtoeva, M. A. Otiev, “Oxidative stress and biochemical markers of endothelial dysfunction and organ damage under conditions of experimental nonferrous metal intoxication”, Bull. Exp. Biol. Med, 162 (2016), 199–202 | DOI
[91] E. Chen, G. Proestou, D. Bourbeau, E. Wang, “Rapid up-regulation of peptide elongation factor EF-1$\alpha$ protein levels is an immediate early event during oxidative stress-induced apoptosis”, Exp. Cell Res, 259 (2000), 140–148 | DOI
[92] M. Alizadeh, M. Wada, C. M. Gelfman, J. T. Handa, L. M. Hjelmeland, “Downregulation of differentiation specific gene expression by oxidative stress in ARPE-19 cells”, Invest. Ophthalmol. Vis. Sci, 42 (2001), 2706–2713
[93] W. B. Tsai, Y. Long, J. R. Park, J. T. Chang, H. Liu, J. Rodriguez-Canales, N. Savaraj, L. G. Feun, M. A. Davies, I. I. Wistuba, M. T. Kuo, “Gas6/Axl is the sensor of arginine-auxotrophic response in targeted chemotherapy with arginine-depleting agents”, Oncogene, 35 (2016), 1632–1642 | DOI
[94] L. A. Gibson, R. A. Lavoie, S. Bissegger, L. M. Campbell, V. S. Langlois, “A positive correlation between mercury and oxidative stress-related gene expression (GPX3 and GSTM3) is measured in female Double-crested Cormorant blood”, Ecotoxicology, 23 (2014), 1004–1014 | DOI
[95] H. Jiao, R. Natoli, K. Valter, J. M. Provis, M. Rutar, “Spatiotemporal cadence of macrophage polarisation in a model of light-induced retinal degeneration”, PLoS One, 10 (2015), e0143952 | DOI
[96] B. Yang, J. Wagner, N. Damaschke, T. Yao, S. M. Wuerzberger-Davis, M. H. Lee, J. Svaren, S. Miyamoto, D. F. Jarrard, “A novel pathway links oxidative stress to loss of Insulin Growth Factor-2 (IGF2) imprinting through NF–B activation”, PLoS One, 9 (2014), e88052 | DOI
[97] S. Joseph Martin, S. Evan Prince, “Comparative modulation of levels of oxidative stress in the liver of anti-tuberculosis drug treated Wistar rats by vitamin B12, beta-carotene, and Spirulina fusiformis: Role of NF-$\kappa$B, iNOS, IL-6, and IL-10”, J. Cell. Biochem, 118 (2017), 3825–3833 | DOI
[98] D. Liu, R. Zhang, J. Wu, Y. Pu, X. Yin, Y. Cheng, J. Wu, C. Feng, Y. Luo, J. Zhang, “Interleukin-promotes esophageal adenocarcinoma cell invasiveness through ROS-dependent, NF-$\kappa$B-mediated MMP-2/9 activation”, Oncol. Rep., 37 (2017), 1779–1785, 17 pp. | DOI
[99] M. Nomura, Y. Yoshimura, T. Kikuiri, T. Hasegawa, Y. Taniguchi, Y. Deyama, K. Koshiro, H. Sano, K. Suzuki, N. Inoue, “Platinum nanoparticles suppress osteoclastogenesis through scavenging of reactive oxygen species produced in RAW264.7 cells”, J. Pharmacol. Sci, 117 (2011), 243–252 | DOI
[100] H. K. Kim, S. H. Hwang, S. Abdi, “Tempol ameliorates and prevents mechanical hyperalgesia in a rat model of chemotherapy-induced neuropathic pain”, Front. Pharmacol, 7 (2017), 532 | DOI
[101] A. D. Lake, C. E. Wood, V. S. Bhat, B. N. Chorley, G. K. Carswell, Y. M. Sey, E. M. Kenyon, B. Padnos, T. M. Moore, A. H. Tennant et al, “Dose and effect thresholds for early key events in a PPAR$\alpha$-mediated mode of action”, Toxicol. Sci, 149 (2016), 312–325 | DOI
[102] B. T. Davis, R. M. Voigt, M. Shaikh, C. B. Forsyth, A. Keshavarzian, “CREB protein mediates alcohol-induced circadian disruption and intestinal permeability”, Alcohol. Clin. Exp. Res, 41 (2017), 2007–2014 | DOI
[103] S. Desai, S. S. Baker, W. Liu, D. A. Moya, R. W. Browne, L. Mastrandrea, R. D. Baker, L. Zhu, “Paraoxonase 1 and oxidative stress in paediatric non-alcoholic steatohepatitis”, Liver Int, 34 (2014), 110–117 | DOI
[104] K. Y. Lee, P. H. Feng, S. C. Ho, K. J. Chuang, T. T. Chen, C. L. Su, W. T. Liu, H. C. Chuang, “Inter-alpha-trypsin inhibitor heavy chain 4: a novel biomarker for environmental exposure to particulate air pollution in patients with chronic obstructive pulmonary disease”, Int. J. Chron. Obstruct. Pulmon. Dis, 10 (2015), 831–841
[105] H. Sasaki, M. Shitara, K. Yokota, Y. Hikosaka, S. Moriyama, M. Yano, Y. Fujii, “RagD gene expression and NRF2 mutations in lung squamous cell carcinomas”, Oncol. Lett, 4 (2012), 1167–1170 | DOI
[106] M. Takano, A. Meneshian, E. Sheikh, Y. Yamakawa, K. B. Wilkins, E. A. Hopkins, G. B. Bulkley, “Rapid upregulation of endothelial P-selectin expression via reactive oxygen species generation”, Am. J. Physiol. Circ. Physiol., 283 (2002), H2054–H2061 | DOI
[107] G. Frühbeck, N. Sáinz, A. Rodríguez, V. Catalán, S. Becerril, B. Ramírez, J. Gómez-Ambrosi, “Leptin administration downregulates the increased expression levels of genes related to oxidative stress and inflammation in the skeletal muscle of ob/ob mice”, Mediators Inflamm, 2010 (2010), 1–15
[108] T. K.D. Vo, M. de Saint-Hubert, G. Morrhaye, P. Godard, V. Geenen, H. J. Martens, F. Debacq-Chainiaux, C. Swine, O. Toussaint, “Transcriptomic biomarkers of the response of hospitalized geriatric patients admitted with heart failure. Comparison to hospitalized geriatric patients with infectious diseases or hip fracture”, Mech. Ageing Dev, 132 (2011), 131–139 | DOI
[109] D. M. van Leeuwen, E. van Agen, R. W. Gottschalk, R. Vlietinck, M. Gielen, M. H. van Herwijnen, L. M. Maas, J. C. Kleinjans, J. H. van Delft, “Cigarette smoke-induced differential gene expression in blood cells from monozygotic twin pairs”, Carcinogenesis, 28 (2006), 691–697 | DOI
[110] M. Li, J. Zhao, Y. Hu, H. Lu, J. Guo, “Oxygen free radicals regulate energy metabolism via AMPK pathway following cerebral ischemia”, Neurol. Res, 32 (2010), 779–784 | DOI
[111] T. Ogino, H. Kobuchi, H. Fujita, A. Matsukawa, K. Utsumi, “Erythroid and megakaryocytic differentiation of K562 erythroleukemic cells by monochloramine”, Free Radic. Res, 48 (2014), 292–302 | DOI
[112] A. Andersson-Sjöland, J. C. Karlsson, K. Rydell-Törmänen, “ROS-induced endothelial stress contributes to pulmonary fibrosis through pericytes and Wnt signaling”, Lab. Investig, 96 (2016), 206–217 | DOI
[113] Y. Liu, R. Lu, J. Gu, Y. Chen, X. Zhang, L. Zhang, H. Wu, W. Hua, J. Zeng, “Aldehyde dehydrogenase 1A1 up-regulates stem cell markers in benzo[a]pyrene-induced malignant transformation of BEAS-2B cells”, Environ. Toxicol. Pharmacol, 45 (2016), 241–250 | DOI
[114] E. A. Stanford, Z. Wang, O. Novikov, F. Mulas, E. Landesman-Bollag, S. Monti, B. W. Smith, D. C. Seldin, G. J. Murphy, D. H. Sherr, “The role of the aryl hydrocarbon receptor in the development of cells with the molecular and functional characteristics of cancer stem-like cells”, BMC Biol, 14 (2016), 20 | DOI
[115] Y. Ma, D. Liu, “Activation of pregnane X receptor by pregnenolone 16 $\alpha$-carbonitrile prevents high-fat diet-induced obesity in AKR/J mice”, PLoS One, 7 (2012), e38734 | DOI
[116] M. Auslander, Y. Yudkovski, V. Chalifa-Caspi, B. Herut, R. Ophir, R. Reinhardt, P. M. Neumann, M. Tom, “Pollution-affected fish hepatic transcriptome and its expression patterns on exposure to cadmium”, Mar. Biotechnol, 10 (2008), 250–261 | DOI
[117] C. B. Lambert, C. Spire, N. Claude, A. Guillouzo, “Dose- and time-dependent effects of phenobarbital on gene expression profiling in human hepatoma HepaRG cells”, Toxicol. Appl. Pharmacol, 234 (2009), 345–360 | DOI
[118] A. Łazarenkow, M. Michalska, M. Mirowski, K. Słomiak, J. Nawrot-Modranka, “The effect of hydrazine derivatives of 3-formylchromones on angiogenic basic fibroblast growth factor and fibroblast growth factor receptor-1 in human melanoma cell line WM-115”, Acta Biochim. Pol, 64 (2017), 585–590 | DOI
[119] H. Bruchova, A. Vasikova, M. Merkerova, A. Milcova, J. Topinka, I. Balascak, A. Pastorkova, R. J. Sram, R. Brdicka, “Effect of maternal tobacco smoke exposure on the placental transcriptome”, Placenta, 31 (2010), 186–191 | DOI
[120] C. Y. Li, H. J. Renaud, C. D. Klaassen, J. Y. Cui, “Age-specific regulation of drug-processing genes in mouse liver by ligands of xenobiotic-sensing transcription factors”, Drug Metab. Dispos, 44 (2016), 1038–1049 | DOI
[121] C. Wohlfahrt-Veje, K. Audouze, S. Brunak, J. P. Antignac, B. le Bizec, A. Juul, N. E. Skakkebaek, K. M. Main, “Polychlorinated dibenzo-p-dioxins, furans, and biphenyls (PCDDs/PCDFs and PCBs) in breast milk and early childhood growth and IGF1”, Reproduction, 147 (2014), 391–399 | DOI
[122] J. Wang, X. Liu, T. Li, C. Liu, Y. Zhao, “Increased hepatic Igf2 gene expression involves C/EBP$\beta$ in TCDD-induced teratogenesis in rats”, Reprod. Toxicol, 32 (2011), 313–321 | DOI
[123] A. Khalil, P. H. Villard, M. A. Dao, R. Burcelin, S. Champion, F. Fouchier, J. F. Savouret, Y. Barra, E. Seree, “Polycyclic aromatic hydrocarbons potentiate high-fat diet effects on intestinal inflammation”, Toxicol. Lett, 196 (2010), 161–167 | DOI
[124] K. A. Pacheco, M. Tarkowski, C. Sterritt, J. Negri, L. J. Rosenwasser, L. Borish, “The influence of diesel exhaust particles on mononuclear phagocytic cell-derived cytokines: IL-10, TGF-beta and IL-1 beta”, Clin. Exp. Immunol, 126 (2001), 374–383 | DOI
[125] S. Kamaraj, P. Anandakumar, S. Jagan, G. Ramakrishnan, T. Devaki, “Modulatory effect of hesperidin on benzo(a)pyrene induced experimental lung carcinogenesis with reference to COX-2, MMP-2 and MMP-9”, Eur. J. Pharmacol, 649 (2010), 320–327 | DOI
[126] W. E. Gato, D. B. Hales, J. C. Means, “Hepatic gene expression analysis of 2-aminoanthracene exposed Fisher-344 rats reveal patterns indicative of liver carcinoma and type 2 diabetes”, J. Toxicol. Sci, 37 (2012), 1001–1016 | DOI
[127] C. D. Yeo, Y. A. Kim, H. Y. Lee, J. W. Kim, S. J. Kim, S. H. Lee, Y. K. Kim, “Roflumilast treatment inhibits lung carcinogenesis in benzo(a)pyrene-induced murine lung cancer model”, Eur. J. Pharmacol, 812 (2017), 189–195 | DOI
[128] C. A. Luckhurst, M. Ratcliffe, L. Stein, M. Furber, S. Botterell, D. Laughton, W. Tomlinson, R. Weaver, K. Chohan, A. Walding, “Synthesis and biological evaluation of N-alkylated 8-oxybenz[c]azepine derivatives as selective PPAR$\delta$ agonists”, Bioorg. Med. Chem. Lett, 21 (2011), 531–536 | DOI
[129] N. Manzella, M. Bracci, S. Staffolani, E. Strafella, V. Rapisarda, M. Valentino, M. Amati, A. Copertaro, L. Santarelli, “Styrene altered clock gene expression in serum-shocked cultured human fibroblasts”, Biosci. Biotechnol. Biochem, 77 (2013), 1296–1298 | DOI
[130] S. D. Sithu, S. Srivastava, M. A. Siddiqui, E. Vladykovskaya, D. W. Riggs, D. J. Conklin, P. Haberzettl, T. E. O-Toole, A. Bhatnagar, S. E. D'Souza, “Exposure to acrolein by inhalation causes platelet activation”, Toxicol. Appl. Pharmacol, 248 (2010), 100–110 | DOI
[131] C. Gouédard, R. Barouki, Y. Morel, “Dietary polyphenols increase paraoxonase 1 gene expression by an aryl hydrocarbon receptor-dependent mechanism”, Mol. Cell. Biol, 24 (2004), 5209–5222 | DOI
[132] D. Brauze, P. Zawierucha, K. Kiwerska, K. Bednarek, M. Oleszak, M. Rydzanicz, M. Jarmuz-Szymczak, “Induction of expression of aryl hydrocarbon receptor-dependent genes in human HepaRG cell line modified by shRNA and treated with $\beta$-naphthoflavone”, Mol. Cell. Biochem, 425 (2017), 59–75 | DOI
[133] E. Hrubá, J. Vondráček, H. Líbalová, J. Topinka, V. Bryja, K. Souček, M. Machala, “Gene expression changes in human prostate carcinoma cells exposed to genotoxic and nongenotoxic aryl hydrocarbon receptor ligands”, Toxicol. Lett, 206 (2011), 178–188 | DOI
[134] G. Pizzino, N. Irrera, M. Cucinotta, G. Pallio, F. Mannino, V. Arcoraci, F. Squadrito, D. Altavilla, A. Bitto, “Oxidative stress: harms and benefits for human health”, Oxid. Med. Cell. Longev, 2017 (2017), 1–13
[135] N. Netzer, H. Gatterer, M. Faulhaber, M. Burtscher, S. Pramsohler, D. Pesta, “Hypoxia, oxidative stress, fat”, Biomolecules, 5 (2015), 1143–1150 | DOI
[136] P. Wigner, P. Czarny, P. Galecki, K. P. Su, T. Sliwinski, “The molecular aspects of oxidative nitrosative stress and the tryptophan catabolites pathway (TRYCATs) as potential causes of depression”, Psychiatry Res, 262 (2018), 566–574 | DOI
[137] D. Ramírez-Ortega, A. Ramiro-Salazar, D. González-Esquivel, C. Ríos, B. Pineda, V. Pérez de la Cruz, “3-Hydroxykynurenine and 3-hydroxyanthranilic acid enhance the toxicity induced by copper in rat astrocyte culture”, Oxid. Med. Cell. Longev, 2017 (2017), 1–12
[138] X. R. Jiang, M. Z. Wrona, G. Dryhurst, “Tryptamine-4,5-dione, a putative endotoxic metabolite of the superoxide-mediated oxidation of serotonin, is a mitochondrial toxin: Possible implications in neurodegenerative brain disorders”, Chem. Res. Toxicol, 12 (1999), 429–436 | DOI
[139] E. Y. Chen, C. M. Tan, Y. Kou, Q. Duan, Z. Wang, G. Meirelles, N. R. Clark, A. Ma'ayan, “Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool”, BMC Bioinformatics, 14 (2013), 128 | DOI
[140] M. V. Kuleshov, M. R. Jones, A. D. Rouillard, N. F. Fernandez, Q. Duan, Z. Wang, S. Koplev, S. L. Jenkins, K. M. Jagodnik, A. Lachmann et al, “Enrichr: a comprehensive gene set enrichment analysis web server 2016 update”, Nucleic Acids Res., 44 (2016), W90–W97 | DOI
[141] K. Takahashi, S. Yamanaka, “Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors”, Cell, 126 (2006), 663–676 | DOI
[142] J. C. D. Heng, Y. L. Orlov, H. H. NG, “Transcription factors for the modulation of pluripotency and reprogramming”, Cold Spring Harb. Symp. Quant. Biol., 75 (2010), 237–244 | DOI
[143] J. Mathieu, Z. Zhang, W. Zhou, A. J. Wang, J. M. Heddleston, C. M. A. Pinna, A. Hubaud, B. Stadler, M. Choi, M. Bar et al, “HIF induces human embryonic stem cell markers in cancer cells”, Cancer Res, 71 (2011), 4640–4652 | DOI
[144] Q. Chang, B. Chen, C. Thakur, Y. Lu, F. Chen, “Arsenic-induced sub-lethal stress reprograms human bronchial epithelial cells to CD61$^-$ cancer stem cells”, Oncotarget, 5 (2014), 1290–1303 | DOI
[145] J. Balvan, J. Gumulec, M. Raudenska, A. Krizova, P. Stepka, P. Babula, R. Kizek, V. Adam, M. Masarik, “Oxidative stress resistance in metastatic prostate cancer: Renewal by self-eating”, PLoS One, 10 (2015), e0145016 | DOI
[146] M. C. Kim, F. J. Cui, Y. Kim, “Hydrogen peroxide promotes epithelial to mesenchymal transition and stemness in human malignant mesothelioma cells”, Asian Pac. J. Cancer Prev., 14 (2013), 3625–3630 | DOI
[147] T. E. Cullingford, M. J. Butler, A. K. Marshall, E. L. Tham, P. H. Sugden, A. Clerk, “Differential regulation of Krüppel-like factor family transcription factor expression in neonatal rat cardiac myocytes: Effects of endothelin-1, oxidative stress and cytokines”, Biochim. Biophys. Acta Mol. Cell Res, 1783 (2008), 1229–1236 | DOI
[148] J. Kang, M. Gemberling, M. Nakamura, F. G. Whitby, H. Handa, W. G. Fairbrother, D. Tantin, “A general mechanism for transcription regulation by Oct1 and Oct4 in response to genotoxic and oxidative stress”, Genes Dev, 23 (2009), 208–222 | DOI
[149] J. Jang, Y. Wang, H. S. Kim, M. A. Lalli, K. S. Kosik, “Nrf2, a regulator of the proteasome, controls self-renewal and pluripotency in human embryonic stem cells”, Stem Cells, 32 (2014), 2616–2625 | DOI
[150] D. J. Peet, T. Kittipassorn, J. P. Wood, G. Chidlow, R. J. Casson, “HIF signalling: The eyes have it”, Exp. Cell Res, 356 (2017), 136–140 | DOI
[151] E. P. Cummins, C. T. Taylor, “Hypoxia-responsive transcription factors”, Pflügers Arch. – Eur. J. Physiol, 450 (2005), 363–371 | DOI
[152] S. H. Lee, S. Manandhar, Y. M. Lee, “Roles of RUNX in hypoxia-induced responses and angiogenesis”, Adv. Exp. Med. Biol, 2017, 449–469 | DOI
[153] L. O. Klotz, H. Steinbrenner, “Cellular adaptation to xenobiotics: Interplay between xenosensors, reactive oxygen species and FOXO transcription factors”, Redox Biol, 13 (2017), 646–654 | DOI
[154] L. Huang, C. Wang, Y. Zhang, M. Wu, Z. Zuo, “Phenanthrene causes ocular developmental toxicity in zebrafish embryos and the possible mechanisms involved”, J. Hazard. Mater, 261 (2013), 172–180 | DOI
[155] B. P. Sullivan, W. Cui, B. L. Copple, J. P. Luyendyk, “Early growth response factor-1 limits biliary fibrosis in a model of xenobiotic-induced cholestasis in mice”, Toxicol. Sci, 126 (2012), 267–274 | DOI
[156] G. Thiel, G. Cibelli, “Regulation of life and death by the zinc finger transcription factor Egr-1”, J. Cell. Physiol, 193 (2002), 287–292 | DOI
[157] N. Araki, K. Ohno, M. Takeyoshi, M. Iida, “Evaluation of a rapid in vitro androgen receptor transcriptional activation assay using AR-EcoScreen$^{\mathrm{TM}}$ cells”, Toxicol. Vitr, 19 (2005), 335–352 | DOI
[158] H. Sies, C. Berndt, D. P. Jones, “Oxidative stress”, Annu. Rev. Biochem, 86 (2017), 715–748 | DOI
[159] S. Nemmiche, “Oxidative signaling response to cadmium exposure”, Toxicol. Sci, 156 (2017), 4–10
[160] J. Zhang, X. Wang, V. Vikash, Q. Ye, D. Wu, Y. Liu, W. Dong, “ROS and ROS-mediated cellular signaling”, Oxid. Med. Cell. Longev, 2016 (2016), 1–18
[161] S. Monzen, E. Tashiro, I. Kashiwakura, “Megakaryocytopoiesis and thrombopoiesis in hematopoietic stem cells exposed to ionizing radiation”, Radiat. Res, 176 (2011), 716–724 | DOI
[162] N. Puri, K. Sodhi, M. Haarstad, D. H. Kim, S. Bohinc, E. Foglio, G. Favero, N. G. Abraham, “Heme induced oxidative stress attenuates sirtuin1 and enhances adipogenesis in mesenchymal stem cells and mouse pre-adipocytes”, J. Cell. Biochem, 113 (2012), 1926–1935 | DOI
[163] Y. Xu, C. Saegusa, A. Schehr, S. Grant, J. A. Whitsett, M. Ikegami, “C/EBP$\alpha$ is required for pulmonary cytoprotection during hyperoxia”, Am. J. Physiol. Cell. Mol. Physiol., 297 (2009), L286–L298 | DOI
[164] T. C. Hour, Y. L. Lai, C. I. Kuan, C. K. Chou, J. M. Wang, H. Y. Tu, H. T. Hu, C.-S. Lin, W. J. Wu, Y. S. Pu et al, “Transcriptional up-regulation of SOD1 by CEBPD: A potential target for cisplatin resistant human urothelial carcinoma cells”, Biochem. Pharmacol, 80 (2010), 325–334 | DOI
[165] S. Banerjee, N. Aykin-Burns, K. J. Krager, S. K. Shah, S. B. Melnyk, M. Hauer-Jensen, S. A. Pawar, “Loss of C/EBP$\delta$ enhances IR-induced cell death by promoting oxidative stress and mitochondrial dysfunction”, Free Radic. Biol. Med, 99 (2016), 296–307 | DOI
[166] J. Wan, H. J. Badham, L. Winn, “The role of c-MYB in benzene-initiated toxicity”, Chem. Biol. Interact, 153-154 (2005), 171–178 | DOI
[167] J. Li, L. Zhao, Y. Zhang, W. Li, X. Duan, J. Chen, Y. Guo, S. Yang, G. Sun, B. Li, “Imbalanced immune responses involving inflammatory molecules and immune-related pathways in the lung of acute and subchronic arsenic-exposed mice”, Environ. Res., 159 (2017), 381–393 | DOI
[168] E. Sakai, M. Morita, M. Ohuchi, M. A. Kido, Y. Fukuma, K. Nishishita, K. Okamoto, K. Itoh, M. Yamamoto, T. Tsukuba, “Effects of deficiency of Kelch-like ECH-associated protein 1 on skeletal organization: a mechanism for diminished nuclear factor of activated T cells cytoplasmic 1 during osteoclastogenesis”, FASEB J., 31 (2017), 4011–4022 | DOI
[169] Q. Li, P. Zhang, X. Yu, Y. Zhao, Q. Li, Y. Zhang, Z. Yang, Y. Xie, P. Xue, S. Sun et al, “Lead transiently promotes granulocyte-macrophage progenitor differentiation and subsequently suppresses common myeloid progenitor differentiation”, Toxicol. Sci, 160 (2017), 268–283 | DOI
[170] J. N. Rich, “Cancer stem cells: Understanding tumor hierarchy and heterogeneity”, Medicine (Baltimore), 95 (2016), S2–S7 | DOI
[171] S. S. Franco, K. Szczesna, M. S. Iliou, M. Al-Qahtani, A. Mobasheri, J. Kobolák, A. Dinnyés, “In vitro models of cancer stem cells and clinical applications”, BMC Cancer, 16 (2016), 738 | DOI
[172] Y. Sakamoto, S. Prudhomme, M. H. Zaman, “Viscoelastic gel-strip model for the simulation of migrating cells”, Ann. Biomed. Eng., 39 (2011), 2735–2749 | DOI
[173] E. Lagasse, “Cancer stem cells with genetic instability: the best vehicle with the best engine for cancer”, Gene Ther, 15 (2008), 136–142 | DOI
[174] B. Franzén, S. Linder, A. A. Alaiya, E. Eriksson, K. Fujioka, A. C. Bergman, H. Jörnvall, G. Auer, “Analysis of polypeptide expression in benign and malignant human breast lesions”, Electrophoresis, 18 (1997), 582–587 | DOI
[175] D. Süsskind, J. Hurst, J. M. Rohrbach, S. Schnichels, “Novel mouse model for primary uveal melanoma: a pilot study”, Clin. Experiment. Ophthalmol, 45 (2017), 192–200 | DOI
[176] A. García-Casas, D. C. García-Olmo, D. García-Olmo, “Further the liquid biopsy: Gathering pieces of the puzzle of genometastasis theory”, World J. Clin. Oncol., 8 (2017), 378–388 | DOI
[177] F. Wen, G. Curlango-Rivera, D. A. Huskey, Z. Xiong, M. C. Hawes, “Visualization of extracellular DNA released during border cell separation from the root cap”, Am. J. Bot., 104 (2017), 970–978 | DOI
[178] G. G. Jinesh, A. M. Kamat, “Blebbishield emergency program: an apoptotic route to cellular transformation”, Cell Death Differ, 23 (2016), 757–758 | DOI
[179] G. G. Jinesh, A. M. Kamat, “The blebbishield emergency program overrides chromosomal instability and phagocytosis checkpoints in cancer stem cells”, Cancer Res, 77 (2017), 6144–6156 | DOI
[180] J. C. Chang, “Cancer stem cells: Role in tumor growth, recurrence, metastasis, and treatment resistance”, Medicine (Baltimore), 95 (2016), S20–S25 | DOI