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临近蛋白质组学鉴定癌细胞膜顺式分子复合物为潜在的癌症靶标。

Proximity proteomics identifies cancer cell membrane cis-molecular complex as a potential cancer target.

机构信息

Department of Biochemistry, Saitama Medical University, Saitama, Japan.

Department of Biochemistry, Kochi University Medical School, Kochi, Japan.

出版信息

Cancer Sci. 2019 Aug;110(8):2607-2619. doi: 10.1111/cas.14108. Epub 2019 Jul 23.

Abstract

Cancer-specific antigens expressed in the cell membrane have been used as targets for several molecular targeted strategies in the last 20 years with remarkable success. To develop more effective cancer treatments, novel targets and strategies for targeted therapies are needed. Here, we examined the cancer cell membrane-resident "cis-bimolecular complex" as a possible cancer target (cis-bimolecular cancer target: BiCAT) using proximity proteomics, a technique that has attracted attention in the last 10 years. BiCAT were detected using a previously developed method termed the enzyme-mediated activation of radical source (EMARS), to label the components proximal to a given cell membrane molecule. EMARS analysis identified some BiCAT, such as close homolog of L1 (CHL1), fibroblast growth factor 3 (FGFR3) and α2 integrin, which are commonly expressed in mouse primary lung cancer cells and human lung squamous cell carcinoma cells. Analysis of cancer specimens from 55 lung cancer patients revealed that CHL1 and α2 integrin were highly co-expressed in almost all cancer tissues compared with normal lung tissues. As an example of BiCAT application, in vitro simulation of effective drug combinations used for multiple drug treatment strategies was performed using reagents targeted to BiCAT molecules. The combination treatment based on BiCAT information moderately suppressed cancer cell proliferation compared with single administration, suggesting that the information about BiCAT in cancer cells is useful for the appropriate selection of the combination among molecular targeted reagents. Thus, BiCAT has the potential to contribute to several molecular targeted strategies in future.

摘要

在过去的 20 年中,细胞膜上表达的肿瘤特异性抗原已被用作几种分子靶向策略的靶点,并取得了显著成功。为了开发更有效的癌症治疗方法,需要寻找新的靶点和靶向治疗策略。在这里,我们使用近十年受到关注的临近蛋白质组学技术,检查了作为可能的癌症靶点的细胞膜驻留“顺式双分子复合物”(顺式双分子癌症靶点:BiCAT)。使用先前开发的酶促自由基源激活(EMARS)方法来标记与特定细胞膜分子相邻的成分,检测到 BiCAT。EMARS 分析鉴定出一些 BiCAT,例如 L1 密切同源物(CHL1)、成纤维细胞生长因子 3(FGFR3)和α2 整合素,它们在小鼠原发性肺癌细胞和人肺鳞癌细胞中普遍表达。对 55 名肺癌患者的癌症样本进行分析显示,与正常肺组织相比,CHL1 和α2 整合素在几乎所有癌症组织中高度共表达。作为 BiCAT 应用的一个例子,使用针对 BiCAT 分子的试剂,模拟了用于多种药物治疗策略的有效药物组合的体外模拟。与单独给药相比,基于 BiCAT 信息的联合治疗适度抑制了癌细胞增殖,表明癌细胞中 BiCAT 的信息对于从分子靶向试剂中适当选择组合是有用的。因此,BiCAT 有可能为未来的几种分子靶向策略做出贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46df/6676139/edd16e4d92e2/CAS-110-2607-g001.jpg

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