期刊文献+

术前新辅助化疗对结肠癌组织中恶性分子表达及根治手术所致创伤程度的影响 被引量:12

Effect of preoperative neoadjuvant chemotherapy on the expression of malignant molecules in colon cancer tissue and the degree of trauma caused by radical operation
下载PDF
导出
摘要 目的:研究术前新辅助化疗对结肠癌组织中恶性分子表达及根治手术所致创伤程度的影响。方法:选择在唐山市丰润区人民医院诊断为结肠癌的患者,随机分为接受XELOX方案新辅助化疗联合结肠癌根治术的XELOX组及接受单纯结肠癌根治术的对照组。采集手术切除的结肠癌组织并检测增殖、凋亡及侵袭基因的表达量,采集血清并检测肝肾功能指标、炎症因子的含量。结果:XELOX组患者手术切除结肠癌病灶中Rac1、PLD2、CHD1L、Snail、Vimentin、N-cadherin的mRNA表达量均显著低于对照组,MS4A12、ASPP2的mRNA表达量均显著高于对照组;手术后1天和3天时,两组血清中ALT、AST、β2-MG、Cys-C、sICAM-1、sVCAM-1、sTM、sE-selectin的含量无显著性差异。结论:术前新辅助化疗能够抑制结肠癌组织中增殖、凋亡及侵袭基因的表达,同时不会增加手术操作的创伤程度。 Objective:To study the effect of preoperative neoadjuvant chemotherapy on the expression of malignant molecules in colon cancer tissue and the degree of trauma caused by radical operation.Methods:Patients who were diagnosed with colon cancer in Fengrun People's Hospital between March2014and February2017were selected and randomly divided into the XELOX group who accepted XELOX neoadjuvant chemotherapy combined with radical operation for colon cancer and the control group who accepted radical operation for colon cancer alone.Surgically removed colon cancer tissue was collected to test the expression of proliferation,apoptosis and invasion genes,and serum was collected to detect the contents of liver and kidney function indicators as well as inflammatory factors.Results:Rac1,PLD2,CHD1L,Snail,Vimentin and N cadherin mRNA expression levels in surgically removed colon cancer lesions of XELOX group were significantly lower than those of control group while MS4A12and ASPP2mRNA expression levels were significantly higher than those of control group;serum ALT,AST,β2MG,Cys C,sICAM1,sVCAM1,sTM and sE selectin contents were not significantly different between the two groups of patients1day and3days after surgery.Conclusion:Preoperative neoadjuvant chemotherapy can inhibit the proliferation,apoptosis and invasion gene expression in colon cancer tissues without increasing the trauma of operation.
作者 王艳成 WANG Yan cheng(Department of Intestinal Surgery, Fengrun People's Hospital of Tangshan in Hebei Province, Tangshan City, Hebei Province, 064000, China)
出处 《海南医学院学报》 CAS 2017年第17期2416-2418,2422,共4页 Journal of Hainan Medical University
基金 河北省社科基金项目(HB2GL047)~~
关键词 结肠癌 新辅助化疗 增殖 凋亡 侵袭 Colon cancer neoadjuvant chemotherapy proliferation apoptosis invasion
  • 相关文献

参考文献3

二级参考文献42

  • 1Sullivan A, Lu X. ASPP: a new family of oncogenes and turnout suppressor genes[J]. Br J Cancer, 2007, 96(2) : 196 -200.
  • 2Ryter SW, Mizumura K, Choi AM. The impact of autophagy on cell death modalities[ J/OL]. Int J Cell Biol, 2014, 2014: 502676.
  • 3Nesic D, Buti L, Lu X, et al. Structure of the Helicobacter pylori CagA oncoprotein bound to the human tumor suppressor ASPP2 [ J ]. Proc Natl Acad Sci U S A, 2014, 111(4) : 1562 -1567.
  • 4Godin-Heymann N, Wang Y, Slee E, et al. Phosphorylation of ASPP'2 by RAS/MAPK pathway is critical for its full pro-apoptotic function[J/OA]. PLoS One, 2013, 8(12) : e82022.
  • 5Schittenhelm MM, Ming B, Ahmut F, et al. Attenuated expression of apoptosis stimulating protein of 1o53-2 (ASPP2) in human acute leukemia is associated with therapy failure [ J/OA ]. PLoS One, 2013, 8(11) : e80193.
  • 6Wang C, Gao C, Chen Y, et al. Expression pattern of the apoptosis- stimulating protein of p53 family in p53 + human breast cancer cell lines[J3. Cancer Cell/nt, 2013, 13(1) : 116.
  • 7Ma L, Chen ZM, Li XY, et al. Nueleostemin and ASPP2 expression is correlated with pituitary adenoma proliferation[ J ]. Oncol Lett, 2013, 6(5) : 1313 -1318.
  • 8Tordella L, Koch S, Salter V, et al. ASPP2 suppresses squamous cell carcinoma via RelA/p65-mediated repression of p63 [ J ]. Proc Natl Acad Sci U S A , 2013, 110(44) : 17969 - 17974.
  • 9Janke K, Brockmeier U, Kuhlmann K, et al. Factor inhibiting HIF-1 ( FIH-1 ) modulates protein interactions of apoptosis-stimulating p53 binding protein 2(ASPP2) [J]. J Cell Sci, 2013, 126(Pt 12): 2629 - 2640.
  • 10Pa, em- S, Katz C, Friedle & Regulatim d ASPP2 imeractin with p53 core domain by an intramolecular autoinhibitory mechanism [J/OA]. PLoS One, 2013, 8(3) : e58470.

共引文献30

同被引文献125

引证文献12

二级引证文献76

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