摘要:黑色素瘤中的桥粒体突变促进细胞增殖和疾病进展

Maayan Baron, T. Ideker
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引用次数: 0

摘要

桥粒是一种跨膜蛋白复合物,在机械应力作用下促进上皮细胞和其他组织的细胞粘附。桥粒的异常表达通常与导致组织完整性受损的发育性疾病有关。最近,在癌症方面也报道了类似的发现;桥粒基因突变已在各种类型的癌症中被观察到,包括皮肤癌、头颈癌和肺癌,然而,大多数表观遗传改变已被用于将桥粒作为肿瘤转移的抑制因子。在这里,我们报道桥粒在7种癌症类型中经常发生突变。在黑色素瘤中,我们发现超过70%的肿瘤在桥粒中存在非同义突变,并且桥粒突变负担与原发肿瘤样本中mRNA表达水平的强烈下降有关(R = -0.23)。突变型和野生型肿瘤之间的差异基因表达分析和功能特征暗示突变细胞在肿瘤发生早期促进细胞增殖。这些结果独特地来自系统级分析,整合了异质肿瘤中的多种蛋白质复合物和多种细胞类型。引用格式:Maayan Baron, Trey Ideker。黑色素瘤的桥粒体突变促进细胞增殖和疾病进展[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要nr 178。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 178: Desmosome mutations in melanoma promote cellular proliferation and disease progression
Desmosomes are transmembrane protein complexes that contribute to cell-cell adhesion in the epithelia and other tissues under mechanical stress. Aberrant desmosome expression is often associated with developmental diseases leading to impaired tissue integrity. Recently, similar findings have been reported in cancer; Mutations in desmosomes genes have been observed in various cancer types including skin cancer, head and neck and lung cancer, however mostly epigenetic alterations have been used to associate desmosomes as suppressors of tumor metastasis. Here, we report that desmosomes are frequently mutated in seven cancer types. In melanoma, we find that over 70% of tumors have non-synonymous mutations in desmosomes, and that the desmosome mutational burden is associated with a strong decrease in mRNA expression levels in primary tumor samples (R = -0.23). Differential gene expression analysis and functional characterizations between mutant and wild-type tumors implicates the mutated cells in promoting cell proliferation at early stages of tumorigenesis. These results emerge uniquely from a systems-level analysis integrating multiple proteins in complexes and multiple cell types in heterogeneous tumors. Citation Format: Maayan Baron, Trey Ideker. Desmosome mutations in melanoma promote cellular proliferation and disease progression [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 178.
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