热蛋白沉积与肿瘤免疫微环境:卵巢癌治疗的新战场

IF 9.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Aihong Wang , Yin Wang , Chenxiang Du , Huilun Yang , Zhengping Wang , Canhui Jin , Michael R. Hamblin
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引用次数: 0

摘要

与宫颈癌或乳腺癌相比,卵巢癌是女性中较少见的肿瘤,但其恶性程度更高,预后更差。尽管治疗手段不断进步,但卵巢癌患者的五年生存率仍只有 50%。由于免疫检查点抑制剂(ICIs)的最新进展,癌症免疫疗法引起了越来越多的关注。热噬是一种高度炎症性的细胞死亡形式,对于连接先天性免疫和适应性免疫至关重要,并参与肿瘤微环境(TME)内的免疫调节。最近的研究表明,化脓过程可促进卵巢癌的免疫治疗,包括嵌合抗原受体 T 细胞(CAR-T)或 ICIs 治疗。此外,炎性体、各种信号通路和lncRNAs都会影响卵巢癌的化脓过程。在此,我们将讨论热蛋白沉积如何影响卵巢癌的发生和发展以及TME。我们还总结了可靶向热噬细胞死亡过程的小分子药物,这些药物可能有助于卵巢癌的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyroptosis and the tumor immune microenvironment: A new battlefield in ovarian cancer treatment

Ovarian cancer is a less common tumor in women compared to cervical or breast cancer, however it is more malignant and has worse outcomes. Ovarian cancer patients still have a five-year survival rate < 50% despite advances in therapy. Due to recent developments in immune checkpoint inhibitors (ICIs), cancer immunotherapy has attracted increased interest. Pyroptosis is a highly inflammatory form of cell death, which is essential for bridging innate and adaptive immunity, and is involved in immune regulation within the tumor microenvironment (TME). Recent research has shown that pyroptosis can promote immunotherapy of ovarian cancer, including treatment with chimeric antigen receptor T-cells (CAR-T) or ICIs. Moreover, inflammasomes, various signaling pathways and lncRNAs can all affect pyroptosis in ovarian cancer. Here we discuss how pyroptosis affects the development and progression of ovarian cancer as well as the TME. We also provide a summary of small molecule drugs that could target pyroptotic cell death processes and may be useful in ovarian cancer therapy.

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来源期刊
Biochimica et biophysica acta. Reviews on cancer
Biochimica et biophysica acta. Reviews on cancer 医学-生化与分子生物学
CiteScore
17.20
自引率
0.00%
发文量
138
审稿时长
33 days
期刊介绍: Biochimica et Biophysica Acta (BBA) - Reviews on Cancer encompasses the entirety of cancer biology and biochemistry, emphasizing oncogenes and tumor suppressor genes, growth-related cell cycle control signaling, carcinogenesis mechanisms, cell transformation, immunologic control mechanisms, genetics of human (mammalian) cancer, control of cell proliferation, genetic and molecular control of organismic development, rational anti-tumor drug design. It publishes mini-reviews and full reviews.
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