期刊文献+

结直肠癌中沉默信息调节因子1与耐药基因的表达及临床意义 被引量:6

Significance of silent information regulator type 1 and multidrug resistance gene in colorectal cancer
下载PDF
导出
摘要 目的研究沉默信息调节因子1(SIRT1)在结直肠癌中的表达,分析SIRT1与结直肠癌患者相关临床病理指标及多药耐药基因P-糖蛋白(P-gp)、谷胱甘肽转移酶π(GST-π)、DNA拓扑异构酶Ⅱ(TOPO-Ⅱ)之间的关系。方法应用免疫组化方法检测60例结直肠癌组织和24例正常结直肠黏膜中SIRT1的表达情况。结果 60例结直肠癌中,SIRT1在结直肠癌中的阳性表达率高于正常结直肠黏膜(P<0.05),60例结直肠癌中,浸润深度T3~T4者比T1~T2者SIRT1阳性表达率高,86.8%vs 42.9%(P<0.05);有淋巴结转移的比无转移的SIRT1阳性表达率高,93.3%vs 70.0%(P<0.05);pTNM分期Ⅱ、Ⅲ、Ⅳ期比Ⅰ期SIRT1阳性表达率高85.7%、83.3%、90.9%vs20.0%(P<0.05);SIRT1表达与结直肠癌浸润深度(r=0.365,P<0.05)、淋巴结转移(r=0.302,P<0.05)、pTNM分期(r=0.292,P<0.01)、p53蛋白的表达(r=0.335,P<0.05)、P-gp的表达(r=0.271,P<0.05)均呈正相关。结论 SIRT1在结直肠癌组织中高表达,且与肿瘤浸润深度、淋巴结转移、临床分期、多药耐药有关,可能参与了结直肠癌的发生发展及耐药,有可能成为结直肠癌恶性程度及预后评估的生物学指标之一。 Objective To investigate the expression of silent information regulator type 1 (SIRT1) and its correlation with clinicopathologic features with the expression of the drug-resistance associated gene P-gp,GST-n and DNA TOPO- ]] in colorectal cancer(CRC). Methods The expression of SIRT1 in 60 colorectal cancer and 24 samples of corresponding normal colorectal tissues was investigated in the method of immunohistochemistry. Results In 60 colorectal cancer tissues,the positive rate of SIRT1 was significantly higher than that of normal colorectal tissues in tumor invasion T3-T4 compared with T1-T2,86.8% vs 42.9% ( P 〈0.05) ;in the lymph node metastasis as compared with that without lymph node metastasis,93.3 % vs 70.0% ( P 〈0.05) ;in the tumor stage II , III , IV compared with tumor stage I ,85.7% ,83.3% ,90.9% vs 20.0%( P 〈0.05). The expression of SIRT1 was positively correlated with tumor invasion( r =0. 365, P d0.05), the lymph node metastasis( r =0. 302, P 〈0.05) ,pTNM tumor stage( r =0. 292, P〈0.01),p53(r=0.335, P〈0.05) and P-gp( r =0. 271, P〈0.05) in colorectal cancer. Conclusion SIRT1 was up-regulated in colorectal cancer and significantly correlated with tumor invasion,lymph node metastasis, pTNM tumor stage, p53 and P-gp. SIRT1 may involve in the development of colorectal cancer and drug resistance, and may be a novel biological parameter to evaluate the malignant degree of colorectal carcinoma and to predict prognosis of colorectal cancer. The expression of SIRT1 may be a significant prognostic indicator for colorectal cancer.
出处 《临床荟萃》 CAS 2012年第24期2145-2148,F0002,共5页 Clinical Focus
关键词 结直肠肿瘤 多药耐药相关蛋白质类 谷胱甘肽转移酶 细胞凋亡 免疫组织化学 colorectal neoplasms multldrug reslstance-associated protelns glutathlone transferase apoptosis immumohistocheznistry silent information regulator type 1
  • 相关文献

参考文献8

  • 1Pruitt K, Zinn R1, Ohm JE, et al. Inhibition of SIRT1 reactivates silenced cancer genes without loss of promoter DNA hypermethylation[J]. PLOS Genet, 2006,2 (3) : e40. 被引量:1
  • 2Chu F, Chou PM, Zheng X, et al. Control of multidrug resistance gene mdrl and cancer resistance to chemotherapy by the longevity gene sirtl [J]. Cancer Res, 2005,65 ( 22 ) : 10183- 10187. 被引量:1
  • 3Ford J,Jiang M, Milner J. Cancer-specific functions of SIRT1 enable human epithelial cancer cell growth and survival[J]. Cancer Res,2005,65(22) : 10457-10463. 被引量:1
  • 4Olmos Y, Brosens JJ, Lam EW. Interplay between SIRT1 proteins and tumor suppressor transcription factors in chemotherapeutic resisitance of cancer[J]. Drug Resist Updat, 2011,14(1):35-44. 被引量:1
  • 5Firestein R,Blander G, Miehan S, et al. The SIRT1 deacetylase suppresses intestinal tumorigenesis and colon cancer growth [J].PLoS ONE,2008,3(4) :e2020. 被引量:1
  • 6Wu M,Wei W,Xiao X,et al. Expression of SIRT1 is associated with lymph node metastasis and poor prognosis in both operable triple-negtive and non-triple-negative breast cancer [J]. Med Oneol,2012,June 4. 被引量:1
  • 7Li Y, Tollefsbol TO. P16 (INK4a)suppression by glucose restriction contributes to human celluar life span extension through SIRTl-mediated epigenetic and genetic mechanism [J]. PLos One,2011,6(2) :e17421. 被引量:1
  • 8Liu T,Liu PY, Marshall GM. The critical role of the class Ⅲ histone deacetylase SIRT1 in cancer[J]. Cancer Res, 2009,69 (5) : 1702-1705. 被引量:1

同被引文献89

  • 1肖宇,马力文,梁莉,张淑兰,张照辉,王墨培,曹宝山.65例Ⅲ期大肠癌辅助化疗后生存分析[J].临床肿瘤学杂志,2007,12(7):529-531. 被引量:5
  • 2SINCLAIR DA, LINL SJ, GUARENTE L. Life-span extension in yeast [ J ]. Science,2006,312 ( 5771 ) : 195 - 197. 被引量:1
  • 3CHAKRABARTI P, ENGLISH T, KARKI S, et al. SIRT1 controls lipolysis in adipocytes via FOXOl-mediated expression of ATGL [J]. J Lipid Res,2011,52(9) :1693 -1701. 被引量:1
  • 4PONUGOTI B, KIM DH, XIAO Z, et al. SIRT1 deacetylates and inhibits SREBP-1C activity in regulation of hepatic lipid metabolism [ J ]. J Biol Chem,2010,285 (44) :33959 - 33970. 被引量:1
  • 5CHEN HC, JENG YM, YUAN RH, et al. SIRT1 promotes tumorigenesis and resistance to chemotherapy in hepatocellular carcinoma and its expression predicts poor prognosis [ J ]. Ann Surg Oncol,2012,19(6) :2011 -2019. 被引量:1
  • 6BRUNET A, SWEENEY LB, STURGILL JF, et al. Stress- dependent regulation of FOXO transcription factors by the SIRT1 deacetylase [ J ]. Science,2004,303 (5666) :2011 - 2015. 被引量:1
  • 7KIM JR, MOON YJ, KWON KS, et al. Expression of SIRT1 and DBC1 is associated with poor prognosis of soft tissue sarcomas [J]. PLoS One,2013,8(9):e74738. 被引量:1
  • 8WU M, WEI W, XIAO X, et al. Expression of SIRT1 is associated with lymph node metastasis and poor prognosis in both operable triple-negative and non-triple-negative breast cancer [ J ]. Med Oncol,2012,29(5 ) :3240 - 3249. 被引量:1
  • 9FENG AN,ZHANG LH, FAN XS, et al. Expression of SIRT1 in gastric cardiac cancer and its clinicopathologic significance [ J ]. Int J Surg Pathol,2011,19(6) :743 -750. 被引量:1
  • 10WU ML, LI H, YU LJ, et al. Short-term resveratrol exposure causes in vitro and in vivo growth inhibition and apoptosis of bladder cancer cells[ J ]. PLoS One,2014,9 (2) : e89806. 被引量:1

引证文献6

二级引证文献16

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