国际肿瘤学杂志››2017,Vol. 44››Issue (6): 476-.doi:10.3760/cma.j.issn.1673-422X.2017.06.019
周启东,蒋光亮,徐可
出版日期:
2017-06-08发布日期:
2017-06-16通讯作者:
徐可 E-mail:drkexu@163.com基金资助:
国家自然科学基金(81372756)
Zhou Qidong, Jiang Guangliang, Xu Ke
Online:
2017-06-08Published:
2017-06-16Contact:
Xu Ke E-mail:drkexu@163.comSupported by:
National Natural Science Foundation of China (81372756)
摘要:糖皮质激素受体(GR)是类固醇激素核受体超家族成员,可介导糖皮质激素等配体信号,调节靶基因转录,发挥生物学活性。GR在肾癌、膀胱癌和前列腺癌三大泌尿系统恶性肿瘤中均有不同程度表达,能影响肿瘤细胞代谢过程,并与肿瘤发生、发展和预后等环节密切相关。GR为泌尿系统恶性肿瘤的靶向治疗和内分泌治疗提供了重要思路。
周启东,蒋光亮,徐可. 糖皮质激素受体在泌尿系统恶性肿瘤中的研究进展[J]. 国际肿瘤学杂志, 2017, 44(6): 476-.
Zhou Qidong, Jiang Guangliang, Xu Ke. Research progress of glucocorticoid receptor in urological malignant tumors[J]. Journal of International Oncology, 2017, 44(6): 476-.
[1] 王德杰, 刘兴国, 张东. 糖皮质激素受体的研究进展[J]. 现代生物医学进展, 2010, 10(8): 1592-1594. DOI: 10.13241/j.cnki.pmb.2010.08.001. [2] Stechschulte LA, Wuescher L, Marino JS, et al. Glucocorticoid receptor β stimulates Akt1 growth pathway by attenuation of PTEN[J]. J Biol Chem, 2014, 289(25): 17885-17894. DOI: 10.1074/jbc.M113.544072. [3] Nicolaides NC, Charmandari E, Chrousos GP, et al. Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligandinduced repression of the human glucocorticoid receptor[J]. BMC Endocr Disord, 2014, 14: 71. DOI: 10.1186/147268231471. [4] Kassi E, Moutsatsou P. Glucocorticoid receptor signaling and prostate cancer[J]. Cancer Lett, 2011, 302(1): 1-10. DOI: 10.1016/j.canlet.2010.10.020. [5] McBeth L, Grabnar M, Selman S, et al. Involvement of the androgen and glucocorticoid receptors in bladder cancer[J]. Int J Endocrinol, 2015, 2015: 384860. DOI: 10.1155/2015/384860. [6] Czarnecka AM, Niedzwiedzka M, Porta C, et al. Hormone signaling pathways as treatment targets in renal cell cancer (review)[J]. Int J Oncol, 2016, 48(6): 2221-2235. DOI: 10.3892/ijo.2016.3460. [7] Yakirevich E, Matoso A, Sabo E, et al. Expression of the glucocorticoid receptor in renal cell neoplasms: an immunohistochemical and quantitative reverse transcriptase polymerase chain reaction study[J]. Hum Pathol, 2011, 42(11): 1684-1692. DOI: 10.1016/j.humpath.2011.01.014. [8] Min KJ, Jang JH, Lee JT, et al. Glucocorticoid receptor antagonist sensitizes TRAILinduced apoptosis in renal carcinoma cells through upregulation of DR5 and downregulation of cFLIP(L) and Bcl2[J]. J Mol Med (Berl), 2012, 90(3): 309-319. DOI: 10.1007/s0010901108218. [9] Jang JH, Min KJ, Kim S, et al. RU486 induces proapoptotic endoplasmic reticulum stress through the induction of CHOP expression by enhancing C/EBPδ expression in human renal carcinoma caki cells[J]. J Cell Biochem, 2016, 117(2): 361-369. DOI: 10.1002/jcb.25278. [10] Huynh TP, Barwe SP, Lee SJ, et al. Glucocorticoids suppress renal cell carcinoma progression by enhancing Na,KATPase beta1 subunit expression[J]. PLoS One, 2015, 10(4): e122442. DOI: 10.1371/journal.pone.0122442. [11] Arai Y, Nonomura N, Nakai Y, et al. The growthinhibitory effects of dexamethasone on renal cell carcinoma in vivo and in vitro[J]. Cancer Invest, 2008, 26(1): 35-40. DOI:10.1080/07357900701638418. [12] Zheng Y, Izumi K, Li Y, et al. Contrary regulation of bladder cancer cell proliferation and invasion by dexamethasonemediated glucocorticoid receptor signals[J]. Mol Cancer Ther, 2012, 11(12): 2621-2632. DOI: 10.1158/15357163.MCT120621. [13] Ishiguro H, Kawahara T, Zheng Y, et al. Differential regulation of bladder cancer growth by various glucocorticoids: corticosterone and prednisone inhibit cell invasion without promoting cell proliferation or reducing cisplatin cytotoxicity[J]. Cancer Chemother Pharmacol, 2014, 74(2): 249-255. DOI: 10.1007/s0028001424967. [14] Zheng Y, Ishiguro H, Ide H, et al. Compound A inhibits bladder cancer growth predominantly via glucocorticoid receptor transrepression[J]. Mol Endocrinol, 2015, 29(10): 1486-1497. DOI: 10.1210/me.20151128. [15] Lesovaya E, Yemelyanov A, Kirsanov K, et al. Combination of a selective activator of the glucocorticoid receptor Compound A with a proteasome inhibitor as a novel strategy for chemotherapy of hematologic malignancies[J]. Cell Cycle, 2013, 12(1): 133-144. DOI: 10.4161/cc.23048. [16] Kashiwagi E, Fujita K, Yamaguchi S, et al. Expression of steroid hormone receptors and its prognostic significance in urothelial carcinoma of the upper urinary tract[J]. Cancer Biol Ther, 2016, 17(11): 1188-1196. DOI: 10.1080/15384047.2016.1235667. [17] Ishiguro H, Kawahara T, Zheng Y, et al. Reduced glucocorticoid receptor expression predicts bladder tumor recurrence and progression[J]. Am J Clin Pathol, 2014, 142(2): 157-164. DOI: 10.1309/AJCPU8UCEZYG4WTV. [18] McBeth L, Nwaneri AC, Grabnar M, et al. Glucocorticoid receptor beta increases migration of human bladder cancer cells[J]. Oncotarget, 2016, 7(19): 27313-27324. DOI: 10.18632/oncotarget.8430. [19] Nwaneri AC, McBeth L, Hinds TD Jr. SweetP inhibition of glucocorticoid receptor β as a potential cancer therapy[J]. Cancer Cell Microenviron, 2016, 3(3). pii: e1362. [20] Hu J, Chen Q. The role of glucocorticoid receptor in prostate cancer progression: from bench to bedside[J]. Int Urol Nephrol, 2016, 49(3): 369-380. DOI: 10.1007/s1125501614768. [21] Isikbay M, Otto K, Kregel S, et al. Glucocorticoid receptor activity contributes to resistance to androgentargeted therapy in prostate cancer[J]. Horm Cancer, 2014, 5(2): 72-89. DOI: 10.1007/s1267201401732. [22] Arora VK, Schenkein E, Murali R, et al. Glucocorticoid receptor confers resistance to antiandrogens by bypassing androgen receptor blockade[J]. Cell, 2013, 155(6): 1309-1322. DOI: 10.1016/j.cell.2013.11.012. [23] Xie N, Cheng H, Lin D, et al. The expression of glucocorticoid receptor is negatively regulated by active androgen receptor signaling in prostate tumors[J]. Int J Cancer, 2015, 136(4): E27-E38. DOI: 10.1002/ijc.29147. [24] Kach J, Conzen SD, Szmulewitz RZ. Targeting the glucocorticoid receptor in breast and prostate cancers[J]. Sci Transl Med, 2015, 7(305): 305ps19. DOI: 10.1126/scitranslmed.aac7531. [25] Carreira S, Romanel A, Goodall J, et al. Tumor clone dynamics in lethal prostate cancer[J]. Sci Transl Med, 2014, 6(254): 254ra125. DOI: 10.1126/scitranslmed.3009448. |
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