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信号传导和转录激活因子3与肿瘤治疗抵抗 被引量:1

Signal transducers and activators of transcription3 andtumor therapeutic resistance
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摘要 治疗抵抗是造成恶性肿瘤复发、远处转移并最终导致患者死亡的最直接原因。当前,亟需新的药物和方法来消除和抑制治疗抵抗的发生,以提高肿瘤患者预后。研究显示,信号传导和转录激活因子3(signal transducers and activators of transcription3,STAT3)的激活与许多肿瘤细胞的治疗抵抗密切相关,抑制STAT3激活可逆转肿瘤细胞对放化疗的抵抗,因此STAT3极有可能成为攻克恶性肿瘤的关键靶点。 Therapeutic resistance, the most important tumor igenic factor responsible for the cancer patients death, is the major cause leading to tumor relapse and metastasis, which poses a great difficulty in choosing therapeutic methods. Therefore, new treatment drugs/modalities are required tode feat treatment-resistant and improve the survival/outcome of tumor patients. Activation of signal transducers and activators of transcription3 (STAT3) has been found associated with initiation of therapeutic resistance and blockage of the activation can avoid the tumor therapeutic resistance. As a result, STAT3 protein has been considered as an ideal therapeutic target forover coming the resistance to cure cancer patients.
出处 《国际耳鼻咽喉头颈外科杂志》 2017年第1期23-26,共4页 International Journal of Otolaryngology-Head and Neck Surgery
基金 河北省应用基础研究计划重点基础研究项目(14967721D),河北省自然科学基金面上项目(H2012505005)联合资助
关键词 肿瘤 STAT3转录因子 治疗抵抗 Neoplasms STAT3 Transcription Factor therapeutic resistance
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  • 1Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 2005; 365: 1687-717.
  • 2A1-Hajj M, Wicha MS, Benito-Hernandez A, Morrison S J, Clarke MF. Prospective identification of tumorigenic breast cancer cells. Proc Natl Acad Sci U S A 2003; 100: 3983-8.
  • 3Patrawala L, Calhoun T, Schneider-Broussard R, Zhou J, Claypool K, Tang DG. Side population is enriched in tu- morigenic, stem-like cancer cells, whereas ABCG2+ and ABCG2- cancer cells are similarly tumorigenic. Cancer Res 2005; 65: 6207-19.
  • 4Ricci-Vitiani L, Lombardi DG, Pilozzi E, Biffoni M, Todaro M, Peschle C, et al. Identification and expansion of human colon-cancer-initiating cells. Nature 2007; 445: 111-5.
  • 5Fillmore CM, Kuperwasser C. Human breast cancer cell lines contain stem-like cells that self-renew, give rise to phenotypically diverse progeny and survive chemo- therapy. Breast Cancer Res 2008; 10: R25.
  • 6Li X, Lewis MT, Huang J, Gutierrez C, Osborne CK, Wu MF, et al. Intrinsic resistance of tumorigenic breast cancer cells to chemotherapy. J Natl Cancer lnst 2008; 100: 672-9.
  • 7Asselin-Labat ML, Shackleton M, Stingl J, Vaillant F, Forrest NC, Eaves CJ, et al. Steroid hormone receptor status of mouse mammary stem cells. J Natl Cancer Inst 2006; 98: 1011-4.
  • 8Sleeman KE, Kendrick H, Robertson D, Isacke CM, Ashworth A, Smalley MJ. Dissociation of estrogen re- ceptor expression and in vivo stem cell activity in the mammary gland. J Cell Bio12007; 176: 19-26.
  • 9Warri AM, Laine AM, Majasuo KE, Alitalo KK, Harko- nen PL. Estrogen suppression of erbB2 expression is associated with increased growth rate of ZR-75-1 human breast cancer cells in vitro and in nude mice. Int J Can- cer 1991; 49: 616-23.
  • 10McClelland RA, Barrow D, Madden TA, Dutkowski CM, Pamment J, Knowlden JM, et al. Enhanced epi-dermal growth factor receptor signaling in MCF7 breast cancer cells after long-term culture in the presence of the pure antiestrogen ICI 182,780 (Faslodex). Endocrinol- ogy 2001; 142: 2776-88.

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