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本文引用的文献

1
Decreased expression of a single tropomyosin isoform, TM5/TM30nm, results in reduction in motility of highly metastatic B16-F10 mouse melanoma cells.单一原肌球蛋白亚型TM5/TM30nm的表达降低,导致高转移性B16-F10小鼠黑色素瘤细胞的运动性降低。
Biochem Biophys Res Commun. 1996 Aug 14;225(2):427-35. doi: 10.1006/bbrc.1996.1190.
2
Expression of transduced tropomyosin 1 cDNA suppresses neoplastic growth of cells transformed by the ras oncogene.转导的原肌球蛋白1 cDNA的表达抑制了由ras癌基因转化的细胞的肿瘤生长。
Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7039-43. doi: 10.1073/pnas.90.15.7039.
3
Identification of novel alternatively spliced isoforms of the tropomyosin-encoding gene, TMnm, in the rat cochlea.大鼠耳蜗中肌动蛋白结合蛋白编码基因TMnm新型可变剪接异构体的鉴定。
Gene. 1994 Jun 10;143(2):251-6. doi: 10.1016/0378-1119(94)90105-8.
4
Isolation of a yeast tropomyosin-related cDNA clone that encodes a novel transmembrane protein having a C-terminal highly basic region.
Biochem Biophys Res Commun. 1994 Mar 30;199(3):1363-71. doi: 10.1006/bbrc.1994.1381.
5
Restoration of microfilament bundle organization in v-raf-transformed NRK cells after transduction with tropomyosin 2 cDNA.用原肌球蛋白2 cDNA转导后,v-raf转化的NRK细胞中微丝束组织的恢复。
Cancer Lett. 1994 Nov 25;87(1):47-53. doi: 10.1016/0304-3835(94)90408-1.
6
Human fibroblast tropomyosin isoforms: characterization of cDNA clones and analysis of tropomyosin isoform expression in human tissues and in normal and transformed cells.人成纤维细胞原肌球蛋白异构体:cDNA克隆的特性及人组织、正常细胞与转化细胞中原肌球蛋白异构体表达分析
Cell Motil Cytoskeleton. 1993;25(3):267-81. doi: 10.1002/cm.970250307.
7
Motility and adhesive properties of high- and low-metastatic murine neoplastic cells.高转移性和低转移性小鼠肿瘤细胞的运动性和黏附特性
Cancer Res. 1984 Feb;44(2):811-24.
8
Structural and functional properties of the non-muscle tropomyosins.非肌肉原肌球蛋白的结构和功能特性
Mol Cell Biochem. 1983;57(2):127-46. doi: 10.1007/BF00849190.
9
Differential expression of tropomyosin forms in the microfilaments isolated from normal and transformed rat cultured cells.原肌球蛋白形式在从正常和转化的大鼠培养细胞中分离出的微丝中的差异表达。
J Biol Chem. 1983 Nov 25;258(22):13954-64.
10
Lack of tropomyosin correlates with the absence of stress fibers in transformed rat kidney cells.原肌球蛋白的缺失与转化的大鼠肾细胞中应力纤维的缺失相关。
Biochim Biophys Acta. 1982 Apr 29;720(2):154-62. doi: 10.1016/0167-4889(82)90007-6.

低分子量原肌球蛋白亚型TM5/TM30nm在转化大鼠成纤维细胞系中的转化相关表达

Transformation-related expression of a low-molecular-mass tropomyosin isoform TM5/TM30nm in transformed rat fibroblastic cell lines.

作者信息

Miyado K, Sato M, Taniguchi S

机构信息

Department of Molecular and Developmental Science, Tokai University, Ischara, Japan.

出版信息

J Cancer Res Clin Oncol. 1997;123(6):331-6. doi: 10.1007/BF01438309.

DOI:10.1007/BF01438309
PMID:9222299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12201513/
Abstract

We cloned a full-length rat TM5/TM30nm cDNA. Using this cDNA as a probe, we demonstrated that expression of TM5/TM30nm mRNA was higher in the tumorigenic rat fibroblastic cell lines SR-3Y1-2 and fos-SR-3Y1-202 than in the normal cell line 3Y1. High expression of TM5/TM30nm protein in SR-3Y1-2 and fos-SR-3Y1-202 cells was also detected by Western blot analysis using anti-TM5/TM30nm antiserum. In addition, the cellular localization of this protein differed between 3Y1 cells and tumorigenic ones. These findings suggest that TM5/TM30nm is involved in malignant transformation of rat fibroblastic cells.

摘要

我们克隆了大鼠TM5/TM30nm的全长cDNA。以该cDNA为探针,我们证明,在致瘤性大鼠成纤维细胞系SR-3Y1-2和fos-SR-3Y1-202中,TM5/TM30nm mRNA的表达高于正常细胞系3Y1。使用抗TM5/TM30nm抗血清进行蛋白质免疫印迹分析,也检测到SR-3Y1-2和fos-SR-3Y1-202细胞中TM5/TM30nm蛋白的高表达。此外,该蛋白在3Y1细胞和致瘤性细胞中的细胞定位有所不同。这些发现表明,TM5/TM30nm参与大鼠成纤维细胞的恶性转化。