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三阴性乳腺癌的遗传异质性、肿瘤微环境与免疫治疗

英文原题:Genetic Heterogeneity, Tumor Microenvironment and Immunotherapy in Triple-Negative Breast Cancer.

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Genetic Heterogeneity, Tumor Microenvironment and Immunotherapy in Triple-Negative Breast Cancer.

PubMed 2022/11/29(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

三阴性乳腺癌的异质性在临床、组织病理学和分子水平上已广为人知。基因组不稳定性和较高的突变率是该类型乳腺癌的另外特征,可能导致新抗原的产生和免疫原性的增强。由于发病年龄早、转移潜能高以及远处复发可能性增加,临床结局较差。

因此,为改善这些患者的治疗选择和预后,已开始努力阐明乳腺癌发生、进展和转移扩散的分子机制。极为复杂且异质的肿瘤免疫微环境由多种细胞类型组成,通常具有紊乱的基因表达。信号通路的改变主要与突变基因相关,包括 p53、PIK3CA 和 MAPK,且这些基因与调控免疫反应的基因呈正相关。

值得注意的是,特定的免疫相关基因可用于预后指数,以评估最有效的管理方案。近期研究结果强调,长链非编码 RNA 在塑造肿瘤微环境形成中也发挥重要作用,并可介导肿瘤免疫逃逸。通过多组学方法识别分子特征以及驱动癌变过程早期阶段的效应通路,是开发靶向癌症治疗和预防新策略的重要步骤。通过重塑宿主免疫系统以根除肿瘤细胞的免疫治疗进展,有望带来新的治疗策略。当前研究聚焦于将免疫检查点抑制与化疗、PARP抑制剂、癌症疫苗或NK 细胞疗法相结合。靶向治疗可能改善治疗反应、消除治疗耐药性并提高患者总体生存率。未来,这些不断发展的进步应应用于个性化医疗和癌症患者的最先进管理。

展开英文摘要原文

Heterogeneity of triple-negative breast cancer is well known at clinical, histopathological, and molecular levels. Genomic instability and greater mutation rates, which may result in the creation of neoantigens and enhanced immunogenicity, are additional characteristics of this breast cancer type. Clinical outcome is poor due to early age of onset, high metastatic potential, and increased likelihood of distant recurrence. Consequently, efforts to elucidate molecular mechanisms of breast cancer development, progression, and metastatic spread have been initiated to improve treatment options and improve outcomes for these patients. The extremely complex and heterogeneous tumor immune microenvironment is made up of several cell types and commonly possesses disorganized gene expression. Altered signaling pathways are mainly associated with mutated genes including p53, PIK3CA , and MAPK , and which are positively correlated with genes regulating immune response. Of note, particular immunity-associated genes could be used in prognostic indexes to assess the most effective management.

Recent findings highlight the fact that long non-coding RNAs also play an important role in shaping tumor microenvironment formation, and can mediate tumor immune evasion. Identification of molecular signatures, through the use of multi-omics approaches, and effector pathways that drive early stages of the carcinogenic process are important steps in developing new strategies for targeted cancer treatment and prevention.

Advances in immunotherapy by remodeling the host immune system to eradicate tumor cells have great promise to lead to novel therapeutic strategies. Current research is focused on combining immune checkpoint inhibition with chemotherapy, PARP inhibitors, cancer vaccines, or natural killer cell therapy.

Targeted therapies may improve therapeutic response, eliminate therapeutic resistance, and improve overall patient survival. In the future, these evolving advancements should be implemented for personalized medicine and state-of-art management of cancer patients.

论文信息

作者
Kudelova E、Smolar M、Holubekova V、Hornakova A、Dvorska D、Lucansky V、Koklesova L、Kudela E
第一作者单位
Clinic of Surgery and Transplant Centre, Jessenius Faculty of Medicine Martin, Comenius University in Bratislava, 03601 Martin, Slovakia.Germany
通讯作者单位
Department of Medical Biology, Jessenius Faculty of Medicine Martin, Comenius University in Bratislava, 03601 Martin, Slovakia.Germany
文献类型
综述
期刊
International journal of molecular sciences2022 Nov 29
原文标识
PubMed 36499265 · DOI 10.3390/ijms232314937