文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

肿瘤微环境重塑:克服三阴性乳腺癌治疗耐药性及创新免疫工程的策略

Remodeling of tumour microenvironment: strategies to overcome therapeutic resistance and innovate immunoengineering in triple-negative breast cancer.

作者信息

Singh Desh Deepak, Haque Shafiul, Kim Youngsun, Han Ihn, Yadav Dharmendra Kumar

机构信息

Amity Institute of Biotechnology, Amity University Rajasthan, Jaipur, India.

Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan, Saudi Arabia.

出版信息

Front Immunol. 2024 Dec 10;15:1455211. doi: 10.3389/fimmu.2024.1455211. eCollection 2024.


DOI:10.3389/fimmu.2024.1455211
PMID:39720730
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11666570/
Abstract

Triple-negative breast cancer (TNBC) stands as the most complex and daunting subtype of breast cancer affecting women globally. Regrettably, treatment options for TNBC remain limited due to its clinical complexity. However, immunotherapy has emerged as a promising avenue, showing success in developing effective therapies for advanced cases and improving patient outcomes. Improving TNBC treatments involves reducing side effects, minimizing systemic toxicity, and enhancing efficacy. Unlike traditional cancer immunotherapy, engineered nonmaterial's can precisely target TNBC, facilitating immune cell access, improving antigen presentation, and triggering lasting immune responses. Nanocarriers with enhanced sensitivity and specificity, specific cellular absorption, and low toxicity are gaining attention. Nanotechnology-driven immunoengineering strategies focus on targeted delivery systems using multifunctional molecules for precise tracking, diagnosis, and therapy in TNBC. This study delves into TNBC's tumour microenvironment (TME) remodeling, therapeutic resistance, and immunoengineering strategies using nanotechnology.

摘要

三阴性乳腺癌(TNBC)是全球影响女性的最复杂、最棘手的乳腺癌亚型。遗憾的是,由于其临床复杂性,TNBC的治疗选择仍然有限。然而,免疫疗法已成为一条有前景的途径,在开发针对晚期病例的有效疗法和改善患者预后方面取得了成功。改进TNBC治疗方法包括减少副作用、将全身毒性降至最低以及提高疗效。与传统的癌症免疫疗法不同,工程化非物质可以精确靶向TNBC,促进免疫细胞进入,改善抗原呈递,并引发持久的免疫反应。具有增强的敏感性和特异性、特定细胞吸收和低毒性的纳米载体正受到关注。纳米技术驱动的免疫工程策略专注于使用多功能分子的靶向递送系统,用于TNBC的精确跟踪、诊断和治疗。本研究深入探讨了TNBC的肿瘤微环境(TME)重塑、治疗抗性以及使用纳米技术的免疫工程策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/63031a99d30c/fimmu-15-1455211-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/6d7eb1fa51a8/fimmu-15-1455211-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/4014c94edc68/fimmu-15-1455211-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/8b741fa65cf5/fimmu-15-1455211-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/93ac97bb426a/fimmu-15-1455211-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/51de9030cdc1/fimmu-15-1455211-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/0b2de3a7cd28/fimmu-15-1455211-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/f98fea624126/fimmu-15-1455211-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/2a9b18e15341/fimmu-15-1455211-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/0ede622a7e31/fimmu-15-1455211-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/663c9f051be3/fimmu-15-1455211-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/63031a99d30c/fimmu-15-1455211-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/6d7eb1fa51a8/fimmu-15-1455211-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/4014c94edc68/fimmu-15-1455211-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/8b741fa65cf5/fimmu-15-1455211-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/93ac97bb426a/fimmu-15-1455211-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/51de9030cdc1/fimmu-15-1455211-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/0b2de3a7cd28/fimmu-15-1455211-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/f98fea624126/fimmu-15-1455211-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/2a9b18e15341/fimmu-15-1455211-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/0ede622a7e31/fimmu-15-1455211-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/663c9f051be3/fimmu-15-1455211-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2357/11666570/63031a99d30c/fimmu-15-1455211-g011.jpg

相似文献

[1]
Remodeling of tumour microenvironment: strategies to overcome therapeutic resistance and innovate immunoengineering in triple-negative breast cancer.

Front Immunol. 2024-12-10

[2]
Immunotherapy for triple-negative breast cancer: Existing challenges and exciting prospects.

Drug Resist Updat. 2017-8-19

[3]
Targeting the tumor immune microenvironment: GPCRs as key regulators in triple-negative breast cancer.

Int Immunopharmacol. 2025-2-6

[4]
Improving efficacy of TNBC immunotherapy: based on analysis and subtyping of immune microenvironment.

Front Immunol. 2024

[5]
Immunotherapeutic interventions of Triple Negative Breast Cancer.

J Transl Med. 2018-5-30

[6]
DNA damage response and neoantigens: A favorable target for triple-negative breast cancer immunotherapy and vaccine development.

Int Rev Cell Mol Biol. 2024

[7]
An update on cancer stem cell survival pathways involved in chemoresistance in triple-negative breast cancer.

Future Oncol. 2025-3

[8]
Recent advances in nanotheranostics for triple negative breast cancer treatment.

J Exp Clin Cancer Res. 2019-10-28

[9]
Triple-negative breast cancer-Role of immunology: A systemic review.

Breast J. 2020-5

[10]
Therapeutic potential of isochlorogenic acid A from in improving immune response and enhancing the efficacy of PD-1/PD-L1 blockade in triple-negative breast cancer.

Front Immunol. 2025-3-5

引用本文的文献

[1]
Capacity of Understanding the Future Approaches in Cancer Treatment by Multiple Models of Artificial Intelligence.

J Cancer Educ. 2025-8-15

[2]
Identifying ATP-Binding Cassette Member B5 as a New Biomarker for Oral Squamous Cell Carcinoma.

Oncol Res. 2025-7-18

本文引用的文献

[1]
Cancer therapeutic potential of hovetrichoside C from Jatropha podagrica on apoptosis of MDA-MB-231 human breast cancer cells.

Food Chem Toxicol. 2024-8

[2]
Macrocyclization strategy for improving candidate profiles in medicinal chemistry.

Eur J Med Chem. 2024-6-5

[3]
CK2α-mediated phosphorylation of GRP94 facilitates the metastatic cascade in triple-negative breast cancer.

Cell Death Discov. 2024-4-22

[4]
Nanoquercetin and Extracellular Vesicles as Potential Anticancer Therapeutics in Hepatocellular Carcinoma.

Cells. 2024-4-5

[5]
MicroRNAs as regulators of immune checkpoints in cancer immunotherapy: targeting PD-1/PD-L1 and CTLA-4 pathways.

Cancer Cell Int. 2024-3-10

[6]
Targeting triple negative breast cancer stem cells using nanocarriers.

Discov Nano. 2024-3-7

[7]
Breaking Barriers: The Promise and Challenges of Immune Checkpoint Inhibitors in Triple-Negative Breast Cancer.

Biomedicines. 2024-2-5

[8]
Targeting Receptor Tyrosine Kinases as a Novel Strategy for the Treatment of Triple-Negative Breast Cancer.

Technol Cancer Res Treat. 2024

[9]
Identification of CD160-TM as a tumor target on triple negative breast cancers: possible therapeutic applications.

Breast Cancer Res. 2024-2-15

[10]
New Insights into the Role of KLF10 in Tissue Fibrosis.

Int J Mol Sci. 2024-1-20

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索