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Published on: May 14, 2021
Targeting Cancer-Associated Fibroblasts: Eliminate or Reprogram?
Masaya Yamazaki1, Takatsugu Ishimoto1,2
1Division of Carcinogenesis, The Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
Abstract:
Cancer-associated fibroblasts (CAFs) are key components of the tumor microenvironment (TME). Given their various roles in tumor progression and treatment resistance, CAFs are promising therapeutic targets in cancer. The elimination of tumor-promoting CAFs has been investigated in various animal models to determine whether it effectively suppresses tumor growth. Based on recent evidence, several simple strategies have been proposed to eliminate tumor-promoting CAFs and attenuate these features. In addition, attention has focused on the critical role that CAFs play in the immunosuppressive TME. Therefore, the functional reprogramming of CAFs in combination with immune checkpoint inhibitors has also been investigated as a possible therapeutic approach. However, although potential targets in CAFs have been widely characterized, the plasticity and heterogeneity of CAFs complicate the understanding of their properties and present difficulties for clinical application. Moreover, the identification of tumor-suppressive CAFs highlights the necessity for the development of therapeutic approaches that can distinguish and switch between tumor-promoting and tumor-suppressive CAFs in an appropriate manner. In this review, we introduce the origins and diversity of CAFs, their role in cancer, and current therapeutic strategies aimed at targeting CAFs, including ongoing clinical evaluations.
Insights
Cancer-associated fibroblasts (CAFs) are crucial in the tumor microenvironment, influencing cancer progression and treatment resistance. Targeting CAFs offers promising therapeutic strategies, but their plasticity requires nuanced approaches for effective cancer treatment.
Area of Science:
- Oncology
- Immunology
- Cell Biology
Background:
- Cancer-associated fibroblasts (CAFs) are integral to the tumor microenvironment (TME).
- CAFs significantly impact tumor progression, metastasis, and resistance to therapies.
- Their dual role in promoting or suppressing tumors necessitates targeted strategies.
Purpose of the Study:
- To review the origins, diversity, and functions of CAFs in cancer.
- To explore current therapeutic strategies targeting CAFs.
- To discuss the challenges and future directions in CAF-targeted cancer therapy.
Main Methods:
- Literature review of preclinical and clinical studies on CAFs.
- Analysis of CAF heterogeneity and plasticity.
- Evaluation of therapeutic approaches including CAF elimination and reprogramming.
Main Results:
- CAFs exhibit significant heterogeneity and plasticity, complicating therapeutic targeting.
- Strategies to eliminate tumor-promoting CAFs show potential in preclinical models.
- Reprogramming CAFs in combination with immunotherapy is an emerging therapeutic avenue.
Conclusions:
- Targeting CAFs presents a promising strategy for cancer treatment.
- Understanding CAF plasticity and heterogeneity is critical for developing effective therapies.
- Future research should focus on developing methods to selectively target tumor-promoting CAFs while sparing tumor-suppressive ones.
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