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西妥昔单抗在结直肠癌中的研究与应用 被引量:2

Cetuximab in the Colorectal Cancer
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摘要 结直肠癌在我国发病呈明显的上升趋势,由于其难以早期发现,患者在接受治疗时往往已经是中晚期,传统的化疗药物不能取得满意的疗效,并且毒副作用明显,患者难以耐受。分子靶向治疗药物以其低毒高效的特点在临床肿瘤治疗中发展迅速,为肿瘤患者个体化治疗开辟了新的道路。表皮生长因子受体(EGFR)在结直肠癌中高表达,它是一种跨膜酪氨酸激酶(TKs)受体,与肿瘤细胞耐药及患者预后密切相关,针对表皮生长因子受体的靶向治疗药物——西妥昔单抗的研发成功为临床结直肠癌的治疗带来了新希望。西妥昔单抗(Cetuximab)是一种嵌合型单克隆抗体,可与肿瘤细胞上的靶向表皮生长因子受体(EGFR)特异性结合,提高肿瘤对化疗的敏感性。本文将就西妥昔单抗在结直肠癌治疗中的作用进行阐述。 The incidence of colorectal cancer (CRC) is dramatically increasing in China. Because it' s difficult to diag- nose early phase C1LC, patients receiving treatment for CRC are often already at the late stage. The efficacy of traditional chemotherapeutic drugs for CRC is limited, and patients are often unable to bear the treatment due to the severe side effects. Molecular targeted therapeutic drugs for cancer therapy have offered a new way to realize the goal of individualized treatment of cancer, as they are of low toxicity and high efficacy. Epidemaal growth factor receptor (EGFP~), a transmembrane tyrosine kinases (TKs) receptor, is highly expressed in C1LC. High expression of EGFR was reported to be associated with tumor cell resistance and poor patient prognosis. The successful development of cetuximab, an EGFR targeted drag, has brought new hope for the treatment of CRC. Cetuximab is a chimeric monoclonal antibody targeting on EGFR. It could specifically bind to EGFR in tumor ceils, so that it can increase the sensitivity of chemotherapy. In this review we mainly focused on the ef- fects ofcetuximab on the treatment of CRC.
机构地区 江西省肿瘤医院
出处 《肿瘤药学》 CAS 2012年第6期407-410,438,共5页 Anti-Tumor Pharmacy
基金 江西省卫生厅重大攻关计划项目资助(20114013)
关键词 西妥昔单抗 表皮生长因子受体 结直肠癌 Cetuximab EGFR Colorectal cancer
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  • 1[1]Majer M,Akerley W,Kuwada SK.Oncologists' current opinion on the treatment of colon carcinoma.Anticancer Agents Med Chem 2007; 7:492-503
  • 2[2]Schulze-Bergkamen H,Krammer PH.Apoptosis in cancerimplications for therapy.Semin Oncol 2004; 31:90-119
  • 3[3]Kroemer G,Reed JC.Mitochondrlal control of cell death.Nat Med 2000; 6:513-519
  • 4[4]Kozopas KM,Yang T,Buchan HL,Zhou P,Craig RW.MCL1,a gene expressed in programmed myeloid cell differentiation,has sequence slinilarity to BCL2.Proc Natl Acad Sci USA 1993; 90:3516-3520
  • 5[5]Rinkenberger JL,Homing S,Klocke B,Roth K,Korsmeyer SJ.Mcl-1 deficiency results in peri-implantation embryonic lethality.Genes Dev 2000; 14:23-27
  • 6[6]Craig RW.MCL1 provides a window on the role of the BCL2 family in cell proliferation,differentiation and tumorigenesis.Leukemia 2002; 16:444-454
  • 7[7]Fleischer B,Schulze-Bergkamen H,Schuchmann M,Weber A,Biesterfeld S,Muller M,Krammer PH,Gaile PR.Mcl-1 is an anti-apoptotic factor for human hepatocellular carcinoma.Int J Oncol 2006; 28:25-32
  • 8[8]Song L,Coppola D,Livingston S,Cress D,Haura EB.Mcl-1 regulates survival and sensitivity to diverse apoptotic stimuli in human non-small cell lung cancer ceils.Cancer Biol Ther 2005; 4:267-276
  • 9[9]Schulze-Bergkamen H,Fleischer B,Schuchmann M,Weber A,Weinmann A,Krammer PH,Galle PR.Suppression of Mcl-1 via RNA interference sensitizes human hepatoceilular carcinoma ceils towards apoptosis induction.BMC Cancer 2006; 6:232
  • 10[10]Han J,Goldstein LA,Gastman BR,Rabinowich H.interrelated roles for Mcl-1 and BIM in regulation of TRAILmediated mitochondrial apoptosis.J Biol Chem 2006; 281:10153-10163

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  • 1邓薇,沈琳.胃癌靶向药物治疗进展[J].中国医学前沿杂志(电子版),2013,5(1):29-41. 被引量:8
  • 2文进,李幼平.Meta分析中效应尺度指标的选择[J].中国循证医学杂志,2007,7(8):606-613. 被引量:128
  • 3Bijnsdorp IV, Kruyt FA, Fukushima M, et al. Molecular mechanism underlying the synergistic interaction between trifluorothymidine and the epidermal growthfactor receptor inhibitor erlotinib in human colorectal cancer cell lines[ J]. Cancer Sci, 2010,101 (2) :440 - 447.
  • 4Tabemero J, Pfeiffer P, Cervantes A. Administration of cetuximab every 2 weeks in the treatment of metastatic colorectal cancer: an effective, more convenient alternative to weekly administration [ J ] ? Oncologist, 2008,13(2) :113 - 119.
  • 5De Reyni~s A, Boige V, Milano G, et al. KRAS mutation signature in colorectal tumors significantly overlaps with the cetuximab response sig- nature [ J ]. J Clin Oncol, 2008,26 ( 13 ) :2228 - 2230.
  • 6Tabernero J, Van Cutsem E, Dlaz - Rubio E, et al. Phase II trial of cetuximab in combination with fluorouracil, leueovorin, and oxaliplatin in the first - line treatment of metastatic eolorectal cancer [ J ]. J Clin Oneol, 2007,25 ( 33 ) :5225 - 5232.
  • 7National Comprehensive Cancer Network. No. 12/09/14. NCCN Clinical Practice Guidelines in Oncology Rectal Cancer Version 2. 2015 [ S]. USA: National Comprehensive Cancer Network. [2015-2-20]. http://guide, medlive. cn/guideline/7460.
  • 8National Comprehensive Cancer Network. No. 10/03/14. NCCN Clinical Practice Guidelines in Oncology Colon Cancer Version 2. 2015 [S]. USA: National Comprehensive Cancer Network. [2015-2-20]. http ://guide. medlive. cn/guideline/7015.
  • 9National Comprehensive Cancer Network. No. 07/01/13. NCCN Clinical Practice Guidelines in Ontology Colorectal Cancer Version 2. 2013 [ S ]. USA: National Comprehensive Cancer Network. [ 2015-2-20]. http://guide, medlive, czr/guideline/preview/1/ 4774.
  • 10Zhang D,Ye J,Xu T, et al. Treatment related severe and fatal ad- verse events with cetuximab in colorectal cancer patients: a meta- analysis[J]. J Chemother, 2013, 25 (3): 170-175.

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