期刊文献+

PinX1在结直肠癌中的表达及预后意义 被引量:3

Expression of PinX 1 protein in colorectal cancer and its clinical significance
原文传递
导出
摘要 目的:探讨PinX1在结直肠癌中的表达及其临床意义。方法收集83例结直肠癌和癌旁组织蜡块,所有患者均接受5-氟尿嘧啶(5-Fu)及其衍生物为基础的辅助化疗4~6个周期,免疫组化检测PinX1蛋白的表达,并分析其与临床病理特征及预后的关系,率的分析采取卡方检验,生存分析应用Kaplan-Meier法和Cox风险比例模型。结果36例(43.4%)癌组织的PinX1蛋白呈低表达,而在相应癌旁组织中,仅8例(9.6%)呈低表达,差异有统计学意义(P<0.05)。尽管PinX1表达下调与临床病理参数无关,经生存分析和Cox风险比例回归模型显示,PinX1表达下调是OS及DFS的独立预后指标。结论PinX1表达下调在结直肠癌发生发展中起重要作用,并可能成为5-Fu辅助化疗结直肠癌患者预后判断指标。 ObjectiveTo explore the expression of PinX1 protein in colorectal cancer (CRC) tissues and its clinical significance.Methods A total of 83 paired CRC specimens and their adjacent normal tissues were collected, all of the patients received 4-6 cycles of 5-fluorouracil (5-Fu) based adjuvant chemotherapy. PinX1 protein expression was analyzed by immunohistochemical staining, its correlations with clinicopathological factors and prognosis were further evaluated.Results PinX1 expression was decreased in 36 tumor tissues (43.4%), while only decreased in 8 adjacent normal tissues (9.6%), which was statistically significant (P〈0.001). Although no correlations with clinicopathological features, PinX1 downregulation was significantly associated with adverse 5-year overall survival (OS) and disease-free survival (DFS).Conclusion PinX1 protein expression is decreased in CRC, which may be a new promising tumor marker for CRC prognosis and 5-FU chemosensitivity.
出处 《中华临床医师杂志(电子版)》 CAS 2015年第17期45-47,共3页 Chinese Journal of Clinicians(Electronic Edition)
基金 皖南医学院中青年科研基金(WK201035F)
关键词 免疫组织化学 结直肠癌 预后 PinX1 Immunohistochemistry Colorectal cancer Prognosis PinX1
  • 相关文献

参考文献15

  • 1Saif MW, Chu E. Biology of colorectal cancer[J]. Cancer J, 2010, 16(3): 196-201.
  • 2Zhou XZ, Lu KP. The Pin2/TRFl-interacting protein PinX1 is a potent telomerase inhibitor[J]. Cell, 2001, 107(3): 347-359.
  • 3Zhang B, Bai YX, Ma HI:/, et al. Silencing PinX1 compromises telomere length maintenance as well as tumorigenicity in telomerase-positive human cancer cells[J]. Cancer Res, 2009, 69(1): 75-83.
  • 4Zhang 1L Zhao J, Wang X, et al. pinX1 without the G-patch motif suppresses proliferation, induces senescence, but does not inhibit telomerase activity in colorectal cancer SW480 cells[J]. Oncol Rep, 2014, 32(1): 286-292.
  • 5Cai MY, Zhang B, He WP, et al. Decreased expression of PinXl protein is correlated with tumor development and is a new independent poor prognostic factor in ovarian carcinoma[J]. Cancer Sci, 2010, 101(6): 1543-1549.
  • 6Wang HB, Wang WQ, Wang XW, et al. PinX1 gene transfection enhances the sensitivity of gastric carcinoma cell line to 5-fluoroumcil[J]. Hepatogastroenterology, 2011, 58(106): 682-686.
  • 7Tian XP, Qian D, He LR, et al. The telomere/telomerase binding factor PinX1 regulates paclitaxel sensitivity depending on spindle assembly checkpoint in human cervical squamons cell carcinomas[J]. Cancer Lett, 2014, 353(1): 104-114.
  • 8Artandi SE, DePinho RA. Telomeres and telomerase in cancer [J]. Carcinogenesis, 2010, 31(1): 9-18.
  • 9Kelland L. Targeting the limitless replieative potential of cancer: the pathway[J]. Clin Cancer Res, 2007, 13(17): 4960-4963.
  • 10Soohoo CY, Shi R, Lee TH, et al. Telomerase inhibitor PINX1 provides a link between TRF1 and telomerase to prevent telomere elongation[J]. J Biol Chem, 201 t, 286(5): 3894-3906.

二级参考文献15

  • 1Saif MW, Chu E. Biology of colorectal cancer[J]. Cancer J, 2010, 16(3): 196-201.
  • 2Zhou XZ, Lu KP. The Pin2/TRFl-interacting protein PinX1 is a potent telomerase inhibitor[J]. Cell, 2001, 107(3): 347-359.
  • 3Zhang B, Bai YX, Ma HI:/, et al. Silencing PinX1 compromises telomere length maintenance as well as tumorigenicity in telomerase-positive human cancer cells[J]. Cancer Res, 2009, 69(1): 75-83.
  • 4Zhang 1L Zhao J, Wang X, et al. pinX1 without the G-patch motif suppresses proliferation, induces senescence, but does not inhibit telomerase activity in colorectal cancer SW480 cells[J]. Oncol Rep, 2014, 32(1): 286-292.
  • 5Cai MY, Zhang B, He WP, et al. Decreased expression of PinXl protein is correlated with tumor development and is a new independent poor prognostic factor in ovarian carcinoma[J]. Cancer Sci, 2010, 101(6): 1543-1549.
  • 6Wang HB, Wang WQ, Wang XW, et al. PinX1 gene transfection enhances the sensitivity of gastric carcinoma cell line to 5-fluoroumcil[J]. Hepatogastroenterology, 2011, 58(106): 682-686.
  • 7Tian XP, Qian D, He LR, et al. The telomere/telomerase binding factor PinX1 regulates paclitaxel sensitivity depending on spindle assembly checkpoint in human cervical squamons cell carcinomas[J]. Cancer Lett, 2014, 353(1): 104-114.
  • 8Artandi SE, DePinho RA. Telomeres and telomerase in cancer [J]. Carcinogenesis, 2010, 31(1): 9-18.
  • 9Kelland L. Targeting the limitless replieative potential of cancer: the pathway[J]. Clin Cancer Res, 2007, 13(17): 4960-4963.
  • 10Soohoo CY, Shi R, Lee TH, et al. Telomerase inhibitor PINX1 provides a link between TRF1 and telomerase to prevent telomere elongation[J]. J Biol Chem, 201 t, 286(5): 3894-3906.

共引文献2

同被引文献25

  • 1冯峰,洪宝发,王晓雄,张彬,白云秀,黄君健.PinX1基因在肾癌组织的表达及临床意义[J].泌尿外科杂志(电子版),2010,2(3):13-18. 被引量:3
  • 2Saif MW, Chu E. Biology of colorectal cancer[J]. Cancer J, 2010, 16(3): 196-201.
  • 3Zhou XZ, Lu KP. The Pin2/TRFl-interacting protein PinX1 is a potent telomerase inhibitor[J]. Cell, 2001, 107(3): 347-359.
  • 4Zhang B, Bai YX, Ma HI:/, et al. Silencing PinX1 compromises telomere length maintenance as well as tumorigenicity in telomerase-positive human cancer cells[J]. Cancer Res, 2009, 69(1): 75-83.
  • 5Zhang 1L Zhao J, Wang X, et al. pinX1 without the G-patch motif suppresses proliferation, induces senescence, but does not inhibit telomerase activity in colorectal cancer SW480 cells[J]. Oncol Rep, 2014, 32(1): 286-292.
  • 6Cai MY, Zhang B, He WP, et al. Decreased expression of PinXl protein is correlated with tumor development and is a new independent poor prognostic factor in ovarian carcinoma[J]. Cancer Sci, 2010, 101(6): 1543-1549.
  • 7Wang HB, Wang WQ, Wang XW, et al. PinX1 gene transfection enhances the sensitivity of gastric carcinoma cell line to 5-fluoroumcil[J]. Hepatogastroenterology, 2011, 58(106): 682-686.
  • 8Tian XP, Qian D, He LR, et al. The telomere/telomerase binding factor PinX1 regulates paclitaxel sensitivity depending on spindle assembly checkpoint in human cervical squamons cell carcinomas[J]. Cancer Lett, 2014, 353(1): 104-114.
  • 9Artandi SE, DePinho RA. Telomeres and telomerase in cancer [J]. Carcinogenesis, 2010, 31(1): 9-18.
  • 10Kelland L. Targeting the limitless replieative potential of cancer: the pathway[J]. Clin Cancer Res, 2007, 13(17): 4960-4963.

引证文献3

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部