Common gene expression patterns responsive to mild temperature hyperthermia in normal human fibroblastic cells

References

• van der Zee J, González González D, van Rhoon GC, van Dijk JD, van Putten WL, Hart AA. Comparison of radiotherapy alone with radiotherapy plus hyperthermia in locally advanced pelvic tumours: A prospective, randomised, multicentre trial. Dutch Deep Hyperthermia Group. Lancet 2000; 355: 1119–1125
   PubMed Web of Science ®Google Scholar
• Wust P, Hildebrandt B, Sreenivasa G, Rau B, Gellermann J, Riess H, et al. Hyperthermia in combined treatment of cancer. Lancet Oncol 2002; 3: 487–497
   PubMed Web of Science ®Google Scholar
• Issels RD. Hyperthermia adds to chemotherapy. Eur J Cancer 2008; 44: 2546–2554
   PubMed Web of Science ®Google Scholar
• Zagar TM, Oleson JR, Vujaskovic Z, Dewhirst MW, Craciunescu OI, Blackwell KL, et al. Hyperthermia combined with radiation therapy for superficial breast cancer and chest wall recurrence: A review of the randomised data. Int J Hyperthermia 2010; 26: 612–617
   PubMed Web of Science ®Google Scholar
• Franckena M. Review of radiotherapy and hyperthermia in primary cervical cancer. Int J Hyperthermia 2012; 28: 543–548
   PubMed Web of Science ®Google Scholar
• Westermann A, Mella O, Van Der Zee J, Jones EL, Van Der Steen-Banasik E, Koper P, et al. Long-term survival data of triple modality treatment of stage IIB-III-IVA cervical cancer with the combination of radiotherapy, chemotherapy and hyperthermia – An update. Int J Hyperthermia 2012; 28: 549–553
   PubMed Web of Science ®Google Scholar
• Dewey WC. Arrhenius relationships from the molecule and cell to the clinic. Int J Hyperthermia 2009; 25: 3–20
   PubMed Web of Science ®Google Scholar
• Yarmolenko PS, Moon EJ, Landon C, Manzoor A, Hochman DW, Viglianti BL, et al. Thresholds for thermal damage to normal tissues: An update. Int J Hyperthermia 2011; 27: 320–343
   PubMed Web of Science ®Google Scholar
• Beachy SH, Repasky EA. Toward establishment of temperature thresholds for immunological impact of heat exposure in humans. Int J Hyperthermia 2011; 27: 344–352
   PubMed Web of Science ®Google Scholar
• Frey B, Weiss EM, Rubner Y, Wunderlich R, Ott OJ, Sauer R, et al. Old and new facts about hyperthermia-induced modulations of the immune system. Int J Hyperthermia 2012; 28: 528–542
   PubMed Web of Science ®Google Scholar
• Lindquist S. The heat-shock response. Annu Rev Biochem 1986; 55: 1151–1191
   PubMed Web of Science ®Google Scholar
• Richter K, Haslbeck M, Buchner J. The heat shock response: Life on the verge of death. Mol Cell 2010; 40: 253–266
   PubMed Web of Science ®Google Scholar
• Nollen EA, Brunsting JF, Roelofsen H, Weber LA, Kampinga HH. In vivo chaperone activity of heat shock protein 70 and thermotolerance. Mol Cell Biol 1999; 19: 2069–2079
   PubMed Web of Science ®Google Scholar
• Beckham JT, Wilmink GJ, Opalenik SR, Mackanos MA, Abraham AA, Takahashi K, et al. Microarray analysis of cellular thermotolerance. Lasers Surg Med 2010; 42: 752–765
   PubMed Web of Science ®Google Scholar
• Cheng L, Smith DJ, Anderson RL, Nagley P. Human neuroblastoma SH-SY5Y cells show increased resistance to hyperthermic stress after differentiation, associated with elevated levels of Hsp72. Int J Hyperthermia 2011; 27: 415–426
   PubMed Web of Science ®Google Scholar
• Lanneau D, Brunet M, Frisan E, Solary E, Fontenay M, Garrido C. Heat shock proteins: Essential proteins for apoptosis regulation. J Cell Mol Med 2008; 12: 743–761
   PubMed Web of Science ®Google Scholar
• Woessmann W, Meng YH, Mivechi NF. An essential role for mitogen-activated protein kinases, ERKs, in preventing heat-induced cell death. J Cell Biochem 1999; 74: 648–662
   PubMed Web of Science ®Google Scholar
• Verheij M, Bose R, Lin XH, Yao B, Jarvis WD, Grant S, et al. Requirement for ceramide-initiated SAPK/JNK signaling in stress-induced apoptosis. Nature 1996; 380: 75–79
   PubMed Web of Science ®Google Scholar
• Gabai VL, Yaglom JA, Volloch V, Meriin AB, Force T, Koutroumanis M, et al. Hsp72-mediated suppression of c-Jun N-terminal kinase is implicated in development of tolerance to caspase-independent cell death. Mol Cell Biol 2000; 20: 6826–6836
   PubMed Web of Science ®Google Scholar
• Xu X, Gupta S, Hu W, McGrath BC, Cavener DR. Hyperthermia induces the ER stress pathway. PLoS One 2011; 6: e23740
   PubMed Web of Science ®Google Scholar
• Pallepati P, Averill-Bates DA. Activation of ER stress and apoptosis by hydrogen peroxide in HeLa cells: Protective role of mild heat preconditioning at 40°C. Biochim Biophys Acta 2011; 1813: 1987–1999
   PubMed Web of Science ®Google Scholar
• Dinh HK, Zhao B, Schuschereba ST, Merrill G, Bowman PD. Gene expression profiling of the response to thermal injury in human cells. Physiol Genomics 2001; 7: 3–13
   PubMed Web of Science ®Google Scholar
• Sonna LA, Gaffin SL, Pratt RE, Cullivan ML, Angel KC, Lilly CM. Effect of acute heat shock on gene expression by human peripheral blood mononuclear cells. J Appl Physiol 2002; 92: 2208–2220
   PubMed Web of Science ®Google Scholar
• Murray JI, Whitfield ML, Trinklein ND, Myers RM, Brown PO, Botstein D. Diverse and specific gene expression responses to stresses in cultured human cells. Mol Biol Cell 2004; 15: 2361–2374
   PubMed Web of Science ®Google Scholar
• Zhou M, Zhang A, Lin B, Liu J, Xu LX. Study of heat shock response of human umbilical vein endothelial cells (HUVECs) using cDNA microarray. Int J Hyperthermia 2007; 23: 225–258
   PubMed Web of Science ®Google Scholar
• Wong HR, Odoms K, Sakthivel B. Divergence of canonical danger signals: The genome-level expression patterns of human mononuclear cells subjected to heat shock or lipopolysaccharide. BMC Immunol 2008; 9: 24
   PubMed Web of Science ®Google Scholar
• Schena M, Shalon D, Heller R, Chai A, Brown PO, Davis RW. Parallel human genome analysis: Microarray-based expression monitoring of 1000 genes. Proc Natl Acad Sci USA 1996; 93: 10614–10619
   PubMed Web of Science ®Google Scholar
• Narita N, Noda I, Ohtsubo T, Fujieda S, Tok uriki M, Saito T, et al. Analysis of heat-shock related gene expression in head-and-neck cancer using cDNA arrays. Int J Radiat Oncol Biol Phys 2002; 53: 190–196
   PubMed Web of Science ®Google Scholar
• Kato N, Kobayashi T, Honda H. Screening of stress enhancer based on analysis of gene expression profiles: Enhancement of hyperthermia-induced tumour necrosis by an MMP-3 inhibitor. Cancer Sci 2003; 94: 644–649
   PubMed Web of Science ®Google Scholar
• Borkamo ED, Dahl O, Bruland O, Fluge O. Global gene expression analyses reveal changes in biological processes after hyperthermia in a rat glioma model. Int J Hyperthermia 2008; 24: 425–441
   PubMed Web of Science ®Google Scholar
• Laramie JM, Chung TP, Brownstein B, Stormo GD, Cobb JP. Transcriptional profiles of human epithelial cells in response to heat: Computational evidence for novel heat shock proteins. Shock 2008; 29: 623–630
   PubMed Web of Science ®Google Scholar
• Tabuchi Y, Takasaki I, Wada S, Zhao QL, Hori T, Nomura T, et al. Genes and genetic networks responsive to mild hyperthermia in human lymphoma U937 cells. Int J Hyperthermia 2008; 24: 613–622
   PubMed Web of Science ®Google Scholar
• Furusawa Y, Tabuchi Y, Wada S, Takasaki I, Ohtsuka K, Kondo T. Identification of biological functions and gene networks regulated by heat stress in U937 human lymphoma cells. Int J Mol Med 2011; 28: 143–151
   PubMed Web of Science ®Google Scholar
• Tabuchi Y, Wada S, Furusawa Y, Ohtsuka K, Kondo T. Gene networks related to the cell death elicited by hyperthermia in human oral squamous cell carcinoma HSC-3 cells. Int J Mol Med 2012; 29: 380–386
   PubMed Web of Science ®Google Scholar
• Furusawa Y, Iizumi T, Fujiwara Y, Zhao QL, Tabuchi Y, Nomura T, et al. Inhibition of checkpoint kinase 1 abrogates G2/M checkpoint activation and promotes apoptosis under heat stress. Apoptosis 2012; 17: 102–112
   PubMed Web of Science ®Google Scholar
• Tabuchi Y, Takasaki I, Doi T, Ishii Y, Sakai H, Kondo T. Genetic networks responsive to sodium butyrate in colonic epithelial cells. FEBS Lett 2006; 580: 3035–3041
   PubMed Web of Science ®Google Scholar
• Ahmed K, Furusawa Y, Tabuchi Y, Emam HF, Piao JL, Hassan MA, et al. Chemical inducers of heat shock proteins derived from medicinal plants and cytoprotective genes response. Int J Hyperthermia 2012; 28: 1–8
   PubMed Web of Science ®Google Scholar
• Westwood JT, Clos J, Wu C. Stress-induced oligomerization and chromosomal relocalization of heat-shock factor. Nature 1991; 353: 822–827
   PubMed Web of Science ®Google Scholar
• Mariner PD, Walters RD, Espinoza CA, Drullinger LF, Wagner SD, Kugel JF, et al. Human Alu RNA is a modular transacting repressor of mRNA transcription during heat shock. Mol Cell 2008; 29: 499–509
   PubMed Web of Science ®Google Scholar
• Spriggs KA, Bushell M, Willis AE. Translational regulation of gene expression during conditions of cell stress. Mol Cell 2010; 40: 228–237
   PubMed Web of Science ®Google Scholar
• Wang XZ, Lawson B, Brewer JW, Zinszner H, Sanjay A, Mi LJ, et al. Signals from the stressed endoplasmic reticulum induce C/EBP-homologous protein (CHOP/GADD153). Mol Cell Biol 1996; 16: 4273–4280
   PubMed Web of Science ®Google Scholar
• Marciniak SJ, Yun CY, Oyadomari S, Novoa I, Zhang Y, Jungreis R, et al. CHOP induces death by promoting protein synthesis and oxidation in the stressed endoplasmic reticulum. Genes Dev 2004; 18: 3066–3077
   PubMed Web of Science ®Google Scholar
• Kokame K, Agarwala KL, Kato H, Miyata T. Herp, a new ubiquitin-like membrane protein induced by endoplasmic reticulum stress. J Biol Chem 2000; 275: 32846–32853
   PubMed Web of Science ®Google Scholar
• Chigurupati S, Wei Z, Belal C, Vandermey M, Kyriazis GA, Arumugam TV, et al. The homocysteine-inducible endoplasmic reticulum stress protein counteracts calcium store depletion and induction of CCAAT enhancer-binding protein homologous protein in a neurotoxin model of Parkinson disease. J Biol Chem 2009; 284: 18323–18333
   PubMed Web of Science ®Google Scholar
• Pyrko P, Schönthal AH, Hofman FM, Chen TC, Lee AS. The unfolded protein response regulator GRP78/BiP as a novel target for increasing chemosensitivity in malignant gliomas. Cancer Res 2007; 67: 9809–9816
   PubMed Web of Science ®Google Scholar
• Birkenfeld AL, Lee HY, Majumdar S, Jurczak MJ, Camporez JP, Jornayvaz FR, et al. Influence of the hepatic eukaryotic initiation factor 2alpha (eIF2alpha) endoplasmic reticulum (ER) stress response pathway on insulin-mediated ER stress and hepatic and peripheral glucose metabolism. J Biol Chem 2011; 286: 36163–36170
   PubMed Web of Science ®Google Scholar
• Sarkar D, Su ZZ, Lebedeva IV, Sauane M, Gopalkrishnan RV, Valerie K, et al. mda-7 (IL-24) Mediates selective apoptosis in human melanoma cells by inducing the coordinated overexpression of the GADD family of genes by means of p38 MAPK. Proc Natl Acad Sci USA 2002; 99: 10054–10059
   PubMed Web of Science ®Google Scholar
• Kim SH, Hwang CI, Juhnn YS, Lee JH, Park WY, Song YS. GADD153 mediates celecoxib-induced apoptosis in cervical cancer cells. Carcinogenesis 2007; 28: 223–231
   PubMedGoogle Scholar
• Fu Y, Li J, Lee AS. GRP78/BiP inhibits endoplasmic reticulum BIK and protects human breast cancer cells against estrogen starvation-induced apoptosis. Cancer Res 2007; 67: 3734–3740
   PubMed Web of Science ®Google Scholar
• Wysoczynski M, Miekus K, Jankowski K, Wanzeck J, Bertolone S, Janowska-Wieczorek A, et al. Leukemia inhibitory factor: A newly identified metastatic factor in rhabdomyosarcomas. Cancer Res 2007; 67: 2131–2140
   Google Scholar
• Yu WH, Woessner JF, Jr, McNeish JD, Stamenkovic I. CD44 anchors the assembly of matrilysin/MMP-7 with heparin-binding epidermal growth factor precursor and ErbB4 and regulates female reproductive organ remodeling. Genes Dev 2002; 16: 307–323
   PubMed Web of Science ®Google Scholar
• Gupta M, Gupta SK, Hoffman B, Liebermann DA. Gadd45a and Gadd45b protect hematopoietic cells from UV-induced apoptosis via distinct signaling pathways, including p38 activation and JNK inhibition. J Biol Chem 2006; 281: 17552–17558
   PubMed Web of Science ®Google Scholar
• Liu X, Lee J, Cooley M, Bhogte E, Hartley S, Glick A. Smad7 but not Smad6 cooperates with oncogenic ras to cause malignant conversion in a mouse model for squamous cell carcinoma. Cancer Res 2003; 63: 7760–7768
   PubMed Web of Science ®Google Scholar
• Deacon K, Knox AJ. Endothelin-1 (ET-1) increases the expression of remodeling genes in vascular smooth muscle through linked calcium and cAMP pathways: Role of a phospholipase A(2)(cPLA(2))/cyclooxygenase-2 (COX-2)/prostacyclin receptor-dependent autocrine loop. J Biol Chem 2010; 285: 25913–25927
   PubMed Web of Science ®Google Scholar