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骨巨细胞瘤:最新的分子发病机制和肿瘤生物学。

Giant cell tumor of bone: updated molecular pathogenesis and tumor biology.

机构信息

Department of Pathology, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, 25440, Republic of Korea.

Department of Pathology, School of Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.

出版信息

Hum Pathol. 2018 Nov;81:1-8. doi: 10.1016/j.humpath.2018.06.017. Epub 2018 Jun 23.

Abstract

Giant cell tumor of bone (GCTB)-related clonal aberrations occur in a background of epigenetic histone modifications (especially the G34W mutation of H3F3A gene) that induce cytogenetic abnormalities. Clonal aberrations are closely linked to the aggressiveness of GCTB. The "neoplastic" mononuclear stromal cells in GCTB express fundamental RANKLs and various chemokines and cytokines associated with monocyte recruitment and "reactive" multinucleated giant cells (osteoclastogenesis). The reciprocal and orchestrated actions between mononuclear stromal cells and multinucleated giant cells help in the understanding of the molecular pathogenesis and tumor biology of GCTB. In the future, novel targets in the updated tumor biology and molecular pathogenesis of GCTB should be explored and scrutinized for the development of systemic therapy.

摘要

骨巨细胞瘤(GCTB)相关的克隆性异常发生在表观遗传组蛋白修饰(特别是 H3F3A 基因的 G34W 突变)的背景下,这些修饰会诱导细胞遗传学异常。克隆性异常与 GCTB 的侵袭性密切相关。GCTB 中的“肿瘤性”单核基质细胞表达基本的 RANKLs 和各种趋化因子和细胞因子,这些因子与单核细胞募集和“反应性”多核巨细胞(破骨细胞形成)有关。单核基质细胞和多核巨细胞之间的相互作用有助于理解 GCTB 的分子发病机制和肿瘤生物学。未来,应在 GCTB 的更新肿瘤生物学和分子发病机制中探索和研究新的靶点,以开发系统治疗方法。

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