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肿瘤进展和治疗耐药中内皮细胞信号传导紊乱。

Disturbed endothelial cell signaling in tumor progression and therapy resistance.

作者信息

Fischer Andreas, Alsina-Sanchis Elisenda

机构信息

Department of Clinical Chemistry, University Medical Center Göttingen, Göttingen University, 37075 Göttingen, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Göttingen, Germany.

Department of Clinical Chemistry, University Medical Center Göttingen, Göttingen University, 37075 Göttingen, Germany.

出版信息

Curr Opin Cell Biol. 2024 Feb;86:102287. doi: 10.1016/j.ceb.2023.102287. Epub 2023 Nov 28.

Abstract

Growth of new blood vessels is considered requisite to cancer progression. Recent findings revealed that in addition to inducing angiogenesis, tumor-derived factors alter endothelial cell gene transcription within the tumor mass but also systemically throughout the body. This subsequently contributes to immunosuppression, altered metabolism, therapy resistance and metastasis. Clinical studies demonstrated that targeting the endothelium can increase the success rate of immunotherapy. Single-cell technologies revealed remarkable organ-specific endothelial heterogeneity that becomes altered by the presence of a tumor. In metastases, endothelial transcription differs remarkably between newly formed and co-opted vessels which may provide a basis for developing new therapies to target endothelial cells and overcome therapy resistance more effectively. This review addresses how cancers impact the endothelium to facilitate tumor progression.

摘要

新血管的生长被认为是癌症进展的必要条件。最近的研究发现,肿瘤衍生因子除了诱导血管生成外,还会改变肿瘤块内以及全身内皮细胞的基因转录。这随后会导致免疫抑制、代谢改变、治疗抵抗和转移。临床研究表明,靶向内皮细胞可以提高免疫治疗的成功率。单细胞技术揭示了显著的器官特异性内皮细胞异质性,这种异质性会因肿瘤的存在而改变。在转移灶中,新形成的血管和被征募的血管之间的内皮转录存在显著差异,这可能为开发针对内皮细胞的新疗法并更有效地克服治疗抵抗提供基础。本综述探讨了癌症如何影响内皮细胞以促进肿瘤进展。

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