Targeting the Tumor-Tumor Microenvironment Crosstalk

被引:20
作者
Badve, Sunil S. S. [1 ]
Gokmen-Polar, Yesim [1 ]
机构
[1] Emory Univ, Dept Pathol & Lab Med, 1364 Clifton Rd,H-184, Atlanta, GA 30322 USA
关键词
Tumor; Tumor microenvironment; interactions; dual targeting; cancer progression; metastasis; RANDOMIZED PHASE-II; PANCREATIC-CANCER; OPEN-LABEL; CELL; MACROPHAGES; IMMUNOTHERAPY; FIBROBLASTS; TRIAL; PD-L1; INFLAMMATION;
D O I
10.1080/14728222.2023.2230362
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Cancer development and progression is a complex process influenced by co-evolution of the cancer cells and their microenvironment. However, traditional anti-cancer therapy is mostly targeted toward cancer cells. To improve the efficacy of cancer drugs, the complex interactions between the tumor (T) and the tumor microenvironment (TME) should be considered while developing therapeutics.Areas covered: The present review article will discuss the components of T-TME as well as the potential to co-target these two distinct elements. We document that these approaches have resulted in success in preventing tumor progression and metastasis, albeit in animal models in some cases. Lastly, it is important to consider the tissue context and tumor type as these could significantly modify the role of these molecules/pathways and hence the overall likelihood of response. Furthermore, we discuss the potential strategies to target the components of tumor microenvironment in anti-cancer therapy. PubMed and ClinicalTrials.gov was searched through May 2023.Expert opinion: The tumor-tumor microenvironment cross talk and heterogeneity are major mechanisms conferring resistance to standard of care. Better understanding of the tissue specific T-TME interactions and dual targeting has the promise of improving cancer control and clinical outcomes.
引用
收藏
页数:11
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