期刊文献+

非小细胞肺癌组织LRP和p53表达及其与新辅助化疗关系的研究 被引量:2

Correlation among expressions of LRP,p53 protein and neoadjuvant chemotherapy response in non-small cell lung cancer
下载PDF
导出
摘要 目的:了解非小细胞肺癌(NSCLC)患者LRP和p53的表达与含铂方案新辅助化疗的疗效以及预后之间的关系。方法:通过免疫组化方法研究43例Ⅲ期NSCLC化疗前后肺癌标本LRP和p53的表达,并分析上述指标的表达与新辅助化疗疗效以及生存期的关系。结果:在化疗前后的成对标本中,化疗后肺癌标本LRP和p53的表达[LRP为74.42%(32/43),p53为72.09%(31/43)],明显高于化疗前[LRP为46.51%(20/43),p53为48.84%(21/43)]。LRP阳性组化疗有效率为40%(8/20),LRP阴性组73.91%(17/23),LRP表达与化疗有效率呈负相关,P=0.033。p53阳性组化疗有效率76.19%(16/21),p53阴性组40.91%(9/22),p53表达与化疗有效率正相关,P=0.031。结论:Ⅲ期NSCLC化疗前LRP和p53表达有助预测含铂方案新辅助化疗的疗效。 OBJECTIVE: To understand the correlation among the expressions of lung resistance-related protein(LRP), p53 protein and the response to platinum-based neoadjuvant chemotherapy in patients with non-small cell lung cancer(NSCLC). METHODS: Pre- and post-chemotherapy immunohistochemical studies of lung cancer specimens were performed on 43 patients with stage Ⅲ NSCLC. The data on response rates were analyzed according to the expressions of LRP and P53. RESULTS: In paired samples before and after chemotherapy specimens, the expressions of LRP and p53 were significantly higher in post-chemotherapy samples [LRP 74.42% (32/43), p53 72.09% (31/43)3 than those pre-chemotherapy [LRP 46.51% (20/43), p53 48.84% (21/43)3. LRP expression significantly correlated inversely with the response to chemotherapy [response rates, 40%(8/20) for LRP-positive and 73. 91% (17/23) for LRP-negative], P= 0. 033. p53 expression correlated significantly with the response to chemotherapy [response rates, 76. 19% (16/21) for p53-positive and 40. 91% (9/22) for p53-negative, P=0. 031]. CONCLUSION: These findings indicate that the expressions of LRP and p53 may be useful to predict platinum-based neoadjuvant chemotherapy response in stage Ⅲ NSCLC.
作者 谢勉 何朝生
出处 《中华肿瘤防治杂志》 CAS 2008年第4期262-264,共3页 Chinese Journal of Cancer Prevention and Treatment
关键词 非小细胞肺/药物疗法 肺耐药蛋白 基因 p53 carcinoma, non-small-cell lung/drug therapy lung resistance-related protein genes, p53
  • 相关文献

参考文献8

  • 1Izquierdo M A, Scheffer G L, Flens M J, et al. Major vault protein LRP-related multidrug resistance[J]. Eur J Cancer, 1996, 32A(6) :979-984.
  • 2吕梅君,王洁,易祥华,李德仁,孔洁,张容轩.肺癌耐药蛋白在非小细胞肺癌中的表达与临床相关性研究[J].中华结核和呼吸杂志,2001,24(8):458-460. 被引量:12
  • 3Thottassery J V, Zambetti G P, Arimori K,et al. p53-dependent regulation of MDR1 gene expression causes selective resistance to chemotherapeutic agents[J]. Proc Natl Acad Sci U S A, 1997,94(20) : 11037- 11042.
  • 4Hawkins D S, Demers G M, Galloway D A. Inactivation of p53 enhance sensitivity to multiple chemotherapeutic agents [J]. Cancer Res,1996,56(4):892-898.
  • 5Li Z H,Zhu Y J,Lit X T, et al. Wild-type p53 gene increases MDR gene expression but decrease drug resistance in an MDR ceil line KBV200[J]. Cancer Lett, 1997,119(2) : 177- 184.
  • 6Harada T, Ogura S, Yamazaki K, et al. Predictive value of expression of P53, Bcl-2 and lung resistance-related protein for response to chemotherapy in non-small ceil lung cancers[J]. Cane er Sci,2003,94(4) :394-399.
  • 7Oshita F, Nishio K, Kameda Y, et al. Increased expression Ievels of p53 correlate with good response to cisplatin-based chemotherapy in non-small ceil lung cancer [J ]. OncoI Rep, 2000, 7(6) :1225-1228.
  • 8Lowe S W, Bodis S, McClatchey A, et al. p53 status and the efficacy of cancer therapy invivo[J]. Science, 1994 ,266(5186): 807-810.

二级参考文献1

  • 1G. V. Scagliotti,S. Novello,G. Selvaggi. Multidrug resistance in non-small-cell lung cancer[J] 1999,Annals of Oncology(5):81~84

共引文献11

同被引文献21

  • 1顾伟,张亚妮,李柏,韩洁,程彬彬,凌昌全.人肝癌BEL-7402/5-FU多药耐药细胞株的建立及其生物学特性观察[J].中西医结合学报,2006,4(3):265-270. 被引量:8
  • 2宋晓荣,姬明丽.LRP的表达与非小细胞肺癌耐药性的关系[J].齐齐哈尔医学院学报,2006,27(4):393-395. 被引量:4
  • 3Parkin D M, Bray F, Ferlay J, et al. Global cancer statistics, 2002[J]. CA CancerJ Clin, 2005, 55(2):74- 108.
  • 4Krishna R, Mayer L D. Multidrug resistance (MDR) in cancer. Mechanisms, reversal using modulators of MDR and the role of MDR modulators in influencing the pharmacokinetics of antican cerdrugs[J]. EurJPharmSci, 2000, 11(4): 265 -283.
  • 5Llovet J M, Ricci S, MazzaferroV, et al. Sorafenib in advanced hepatocellular carcinoma[J]. N Engl J Med, 2008, 359 (4): 378-390.
  • 6Cheng A L, Kang Y K, Chen Z, et al. Eficicacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, double-blind, placebo-controlled trial[J]. Lancet Oncol, 2009, 10(1) : 25-34.
  • 7Richly H, Schultheis B, Adamietz I A, et al. Combination of sorafenib and doxorubicin in patients with advanced hepatocellular carcinoma: results from a phase I extension trial[J]. Eur J Cancer, 2009, 45(4):579-587.
  • 8Shi L X, Ma R, Lu R, et al. Reversal effect of tyroservatide (YSV) tripeptide on multi-drug resistance in resistant human hepatocellular carcinoma cell line BEL-7402/5-FU[J]. Cancer Lett, 2008, 269(1): 101 -110.
  • 9Perez-Tomas R. Multidrug resistance:retrospect and prospects in anti-cancer drug treatment[J]. Curr Med Chem, 2006, 13 (16) :1859 -1876.
  • 10Azzariti A, Porcelli L, Simone G M, et al. Tyrosine kinase inhibitors and multidrug resistance proteins:interactions and biological consequences[J]. Cancer Chemother Pharmacol, 2009, 65: 335-346.

引证文献2

二级引证文献9

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