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中华结直肠疾病电子杂志 ›› 2018, Vol. 07 ›› Issue (06) : 572 -575. doi: 10.3877/cma.j.issn.2095-3224.2018.06.013

所属专题: 文献

综述

iRGD肽协同奥沙利铂逆转结直肠肿瘤耐药的研究进展
纪忠伟1, 杨羽茜1, 李胜龙1, 张博淼1, 李云龙1, 黄跃南1,()   
  1. 1. 150086 哈尔滨医科大学附属第二医院普外科
  • 收稿日期:2018-03-28 出版日期:2018-12-25
  • 通信作者: 黄跃南
  • 基金资助:
    黑龙江省教育厅科学技术研究项目(No.12541303)

Advances in research of iRGD peptide cooperating with oxaliplatin in reversing colorectal cancer drug resistance

Zhongwei Ji1, Yuxi Yang1, Shenglong Li1, Bomiao Zhang1, Yunlong Li1, Yuenan Huang1,()   

  1. 1. Department of General Surgery, the Second Affiliated Hospital of Medical University, Harbin 150086, China
  • Received:2018-03-28 Published:2018-12-25
  • Corresponding author: Yuenan Huang
  • About author:
    Corresponding author: Huang Yuenan, Email:
引用本文:

纪忠伟, 杨羽茜, 李胜龙, 张博淼, 李云龙, 黄跃南. iRGD肽协同奥沙利铂逆转结直肠肿瘤耐药的研究进展[J/OL]. 中华结直肠疾病电子杂志, 2018, 07(06): 572-575.

Zhongwei Ji, Yuxi Yang, Shenglong Li, Bomiao Zhang, Yunlong Li, Yuenan Huang. Advances in research of iRGD peptide cooperating with oxaliplatin in reversing colorectal cancer drug resistance[J/OL]. Chinese Journal of Colorectal Diseases(Electronic Edition), 2018, 07(06): 572-575.

结直肠癌是世界上常见的恶性肿瘤,奥沙利铂(oxaliplatin)是常用于结直肠肿瘤化疗的第三代铂类药物,以其为基础的化疗方案现已成为结直肠癌化疗的标准方案。结直肠癌化疗无效的一个重要原因是肿瘤细胞对化疗药物产生耐药,最近研究发现,具有靶向能力的修饰物与化疗药物结合,能提高肿瘤组织内化疗药物的局部浓度。iRGD肽作为一种靶向肽与化疗药物结合,能增强化疗效果,血管内注射与iRGD肽偶联修饰过的化疗药物,能导致化疗药物与肿瘤血管结合,并能扩散到血管外的肿瘤实质。本文就iRGD肽协同奥沙利铂逆转结直肠肿瘤耐药的研究进展做详尽综述。

Colorectal cancer is a common malignant tumor in the world. Oxaliplatin is the third-generation platinum drug and commonly used in colorectal cancer, its chemotherapy-based regimen has become the standard for chemotherapy for colorectal cancer. An important reason of colorectal cancer chemotherapy failure is the development of drug resistance of tumor cells to chemotherapy drugs. Recent studies have found that the combination of targeting modifiers and chemotherapeutic drugs can increase the local concentration of chemotherapeutic drugs in the tumor tissue. iRGD peptide, as a mediator in combination with chemotherapeutic drugs, potentiates the chemotherapeutic effect, intravascular injection of a chemotherapeutic drug modified with the iRGD peptide can cause the chemotherapeutic drug to bind to the tumor blood vessel and spread to the extravascular tumor mass. In this paper, advances in research of iRGD peptide cooperating with oxaliplatin in reversing colorectal cancer drug resistance are reviewed in detail.

[1]
McQuade RM, Stojanovska V, Bornstein JC. Colorectal cancer chemotherapy: the evolution of treatment and new approaches [J].Current medicinalchemistry, 2017, 24(15): 1537-1557.
[2]
Raymond E, Faivre S, Chaney S, et al. Cellular and molecular pharmacology of oxaliplatin [J]. Molecular Cancer Therapeutics, 2002, 1(3): 227-235.
[3]
Mort R, Mo L, McEwan C, et al. Lack of involvement of nucleotide excision repair gene polymorphisms in colorectal cancer [J]. British Journal of Cancer, 2003, 89(2): 333-337.
[4]
Usanova S, Piée-Staffa A, Sied U, et al.Cisplatin sensitivity of testis tumour cells is due to deficiency in interstrand-crosslink repair and low ERCC1-XPF expression [J].Mol cancer, 2010, 9: 248.
[5]
Stordal B, Davey R.ERCC1 expression and RAD51B activity correlate with cell cycle response to platinum drug treatment not DNA repair [J].Cancer Chemother Pharmacol, 2009, 63(4): 661-672.
[6]
Stiegelbauer V, Perakis S, Deutsch A, et al. MicroRNAs as novel predictive biomarkers and therapeutic targets in colorectal cancer [J]. World J Gastroenterol, 2014, 20(33): 11727-11735.
[7]
Kjersem JB, Ikdahl T, Lingjaerde OC, et al. Plasma microRNAs predicting clinical outcome in metastatic colorectal cancer patients receiving first-line oxaliplatin-based treatment [J]. Mol Oncol, 2014, 8(1): 59-67.
[8]
Beretta GL, Benedetti V, Cossa G, et al. Increased levels and defective glycosylation of MRPs in ovarian carcinoma cells resistant to oxaliplatin [J].Biochem Pharmacol, 2010, 79(8): 1108-1117.
[9]
Sugahara KN, Teesalu T, Karmali PP, et al. Tissue-penetrating delivery of compounds and nanoparticles into tumors [J].Cancer Cell, 2009, 16(6): 510-520.
[10]
Ye Y, Zhu L, Ma Y, et al. Synthesis and evaluation of new iRGD peptide analogs for tumor optical imaging [J]. Bioorg Med Chem Lett, 2011, 21(4): 1146-1150.
[11]
Teesalu T, Sugahara KN, Ruoslahti E. Tumor-penetrating peptides [J]. Frontiers in oncology, 2013, 3: 216.
[12]
Alberici L, Roth L, Sugahara KN, et al. De novo design of a tumor-penetrating peptide [J]. Cancer Research, 2013, 73(2): 804-812.
[13]
Teesalu T, Sugahara KN, Kotamraju VR, et al.C-end rule peptides mediate neuropilin-1-dependent cell, vascular, and tissue penetration [J].Proc Natl Acad Sci U S A., 2009, 106(38): 16157-16162.
[14]
Zanuy D, Kotla R, Nussinov R, et al.Sequence dependence of C-end rule peptides in binding and activation of neuropilin-1 receptor [J].J Struct Biol, 2013, 182(2): 78-86.
[15]
Prud′homme GJ, Glinka Y.Neuropilins are multifunctional coreceptors involved in tumor initiation, growth, metastasis and immunity [J].Oncotarget, 2012, 3(9): 921-939.
[16]
Pang HB, Braun GB, Friman T, et al.An endocytosis pathway initiated through neuropilin-1 and regulated by nutrient availability [J].Nat Commun, 2014, 5: 4904.
[17]
Ruoslahti E.Tumor penetrating peptides for improved drug delivery [J].Adv Drug Deliv Rev,2017, 110-111: 3-12.
[18]
Sugahara KN, Teesalu T, Karmali PP, et al.Coadministration of a tumor-penetrating peptide enhances the efficacy of cancer drugs[J].Science, 2010, 328(5981): 1031-1035.
[19]
Thayanithy V, Dickson EL, Steer C, et al.Tumor-stromal cross talk: direct cell-to-cell transfer of oncogenic microRNAs via tunneling nanotubes [J].Trans Res, 2014, 164(5): 359-365.
[20]
Connor Y, Tekleab S, Nandakumar S, et al.Physical nanoscale conduit-mediated communication between tumour cells and the endothelium modulates endothelial phenotype [J].Nat commun, 2015, 6: 8671.
[21]
Sugahara KN, Braun GB, de Mendoza TH, et al.Tumor-penetrating iRGD peptide inhibits metastasis [J].Mol Cancer Ther, 2015, 14(1): 120-128.
[22]
Maione F, Capano S, Regano D, et al.Semaphorin 3A overcomes cancer hypoxia and metastatic dissemination induced by antiangiogenic treatment in mice [J]. J Clin Invest, 2012, 122(5): 1832-1848.
[23]
Carmeliet P, Jain RK. Principles and mechanisms of vessel normalization for cancer and other angiogenic diseases [J].Nat Rev Drug Discov, 2011, 10(6): 417-427.
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