Proteomics and Molecular Cell Physiology Laboratory, Department of Zoology, School of Life Sciences, Bharathiar University, Coimbatore, TN, India.
J Cancer Res Clin Oncol. 2012 May;138(5):827-35. doi: 10.1007/s00432-012-1157-7. Epub 2012 Jan 25.
The aim of this study was to investigate the expression of cPLA(2)α in non-small lung cancer cell lines and tissues, and we sought to determine the in vitro effects of the pyrrolidine-2 inhibitor on cPLA(2)α sensitivity in three different non-small lung cancer cell lines.
The expression of cPLA(2)α was determined in lung cancer cells by Western blot. Cytotoxicity, cell growth and inhibition of cPLA(2)α activity were determined in relation to the concentration of pyrrolidine-2. Finally, this study investigated immunohistochemical expressions of cPLA(2)α in 23 species of human non-small lung cancer and 5 species of human normal lung to assess their clinicopathological relevance.
cPLA(2)α is expressed in A549 and H460, however, no expression in H661 cells. Pyrrolidine-2 demonstrated a dose-dependent inhibitory effect on cell growth and its significantly inhibited BrdU incorporation of human non-small lung cancer cells. Inhibition with pyrrolidine-2 results in reduction in cPLA(2)α activity in A549 and H460 lung cancer cells by 50% when present at IC(50) concentration in arachidonoyl thio-PC assay. Immunohistochemistry of human lung tissue revealed that cPLA(2)α is increased in lung cancer tissues.
Pyrrolidine-2 is a more potent and specific cPLA(2)α inhibitor than MAFP and AACOCF3 and represents an excellent pharmacological tool to investigate the biosynthesis and the biological roles of cancer. The present study suggests that pyrrolidine-2 could be a potential therapeutic agent for cancer therapy.
本研究旨在探讨非小细胞肺癌细胞系和组织中 cPLA(2)α 的表达,并确定吡咯烷-2 抑制剂在三种不同非小细胞肺癌细胞系中对 cPLA(2)α 敏感性的体外作用。
通过 Western blot 测定肺癌细胞中 cPLA(2)α 的表达。测定吡咯烷-2 浓度与细胞毒性、细胞生长和 cPLA(2)α 活性抑制的关系。最后,本研究检测了 23 种人类非小细胞肺癌和 5 种人类正常肺组织中 cPLA(2)α 的免疫组织化学表达,以评估其与临床病理的相关性。
cPLA(2)α 在 A549 和 H460 中表达,而在 H661 细胞中不表达。吡咯烷-2 对细胞生长表现出剂量依赖性抑制作用,并且显著抑制人类非小细胞肺癌细胞的 BrdU 掺入。在 Arachidonoyl Thio-PC 测定中,当吡咯烷-2 存在于 IC(50)浓度时,其对 A549 和 H460 肺癌细胞中 cPLA(2)α 活性的抑制作用降低 50%。人肺组织的免疫组织化学显示,cPLA(2)α 在肺癌组织中增加。
吡咯烷-2 是一种比 MAFP 和 AACOCF3 更有效和特异的 cPLA(2)α 抑制剂,是研究癌症生物合成和生物学作用的理想药理学工具。本研究表明,吡咯烷-2 可能是癌症治疗的潜在治疗剂。