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肺癌肿瘤抑制因子TSLC1与果蝇肿瘤抑制因子Dlg的人类同源物MPP3的关联。

Association of a lung tumor suppressor TSLC1 with MPP3, a human homologue of Drosophila tumor suppressor Dlg.

作者信息

Fukuhara Hiroshi, Masuda Mari, Yageta Mika, Fukami Takeshi, Kuramochi Masami, Maruyama Tomoko, Kitamura Tadaichi, Murakami Yoshinori

机构信息

Tumor Suppression & Functional Genomics Project, National Cancer Center Research Institute, 5-1-1, Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.

出版信息

Oncogene. 2003 Sep 18;22(40):6160-5. doi: 10.1038/sj.onc.1206744.

Abstract

We have previously identified the tumor suppressor in lung cancer 1 (TSLC1) gene as a novel tumor suppressor in human non-small cell lung cancer (NSCLC) by functional complementation. TSLC1 encodes a membrane glycoprotein belonging to an immunoglobulin superfamily and participates in cell adhesion. A truncating mutation of the TSLC1 corresponding to its cytoplasmic domain in a primary NSCLC tumor suggests that this domain is important for tumor suppressor activity. Here, we report that TSLC1 directly associates with MPP3, one of the human homologues of a Drosophila tumor suppressor gene, Discs large (Dlg). This interaction was dependent on the presence of a PDZ-binding motif at the carboxyl terminus of TSLC1. Furthermore, TSLC1 and MPP3 were colocalized at the cell-cell attachment sites in both a low and a high cell density. The MPP3 gene was expressed in normal lung as well as in many tissues examined except for peripheral blood lymphocytes but lost its expression in one of the nine NSCLC cell lines. These results suggest that TSLC1 and MPP3 are involved in the same cascade of cell-cell interaction, and that the disruption of this cascade might lead cells to malignant growth and tumor formation in lung cancer.

摘要

我们之前通过功能互补将肺癌肿瘤抑制因子1(TSLC1)基因鉴定为人类非小细胞肺癌(NSCLC)中的一种新型肿瘤抑制因子。TSLC1编码一种属于免疫球蛋白超家族的膜糖蛋白,并参与细胞黏附。原发性NSCLC肿瘤中TSLC1对应其胞质结构域的截短突变表明该结构域对肿瘤抑制活性很重要。在此,我们报告TSLC1直接与MPP3相互作用,MPP3是果蝇肿瘤抑制基因盘大(Dlg)的人类同源物之一。这种相互作用依赖于TSLC1羧基末端存在的PDZ结合基序。此外,TSLC1和MPP3在低细胞密度和高细胞密度下均共定位于细胞间附着位点。MPP3基因在正常肺组织以及除外周血淋巴细胞外的许多检测组织中均有表达,但在9个NSCLC细胞系之一中失去了表达。这些结果表明TSLC1和MPP3参与了相同的细胞间相互作用级联反应,并且该级联反应的破坏可能导致细胞在肺癌中发生恶性生长和肿瘤形成。

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