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      Define cancer-associated fibroblasts (CAFs) in the tumor microenvironment: new opportunities in cancer immunotherapy and advances in clinical trials

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          Abstract

          Despite centuries since the discovery and study of cancer, cancer is still a lethal and intractable health issue worldwide. Cancer-associated fibroblasts (CAFs) have gained much attention as a pivotal component of the tumor microenvironment. The versatility and sophisticated mechanisms of CAFs in facilitating cancer progression have been elucidated extensively, including promoting cancer angiogenesis and metastasis, inducing drug resistance, reshaping the extracellular matrix, and developing an immunosuppressive microenvironment. Owing to their robust tumor-promoting function, CAFs are considered a promising target for oncotherapy. However, CAFs are a highly heterogeneous group of cells. Some subpopulations exert an inhibitory role in tumor growth, which implies that CAF-targeting approaches must be more precise and individualized. This review comprehensively summarize the origin, phenotypical, and functional heterogeneity of CAFs. More importantly, we underscore advances in strategies and clinical trials to target CAF in various cancers, and we also summarize progressions of CAF in cancer immunotherapy.

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          Hallmarks of Cancer: The Next Generation

          The hallmarks of cancer comprise six biological capabilities acquired during the multistep development of human tumors. The hallmarks constitute an organizing principle for rationalizing the complexities of neoplastic disease. They include sustaining proliferative signaling, evading growth suppressors, resisting cell death, enabling replicative immortality, inducing angiogenesis, and activating invasion and metastasis. Underlying these hallmarks are genome instability, which generates the genetic diversity that expedites their acquisition, and inflammation, which fosters multiple hallmark functions. Conceptual progress in the last decade has added two emerging hallmarks of potential generality to this list-reprogramming of energy metabolism and evading immune destruction. In addition to cancer cells, tumors exhibit another dimension of complexity: they contain a repertoire of recruited, ostensibly normal cells that contribute to the acquisition of hallmark traits by creating the "tumor microenvironment." Recognition of the widespread applicability of these concepts will increasingly affect the development of new means to treat human cancer. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Colorectal cancer

            Several decades ago, colorectal cancer was infrequently diagnosed. Nowadays, it is the world's fourth most deadly cancer with almost 900 000 deaths annually. Besides an ageing population and dietary habits of high-income countries, unfavourable risk factors such as obesity, lack of physical exercise, and smoking increase the risk of colorectal cancer. Advancements in pathophysiological understanding have increased the array of treatment options for local and advanced disease leading to individual treatment plans. Treatments include endoscopic and surgical local excision, downstaging preoperative radiotherapy and systemic therapy, extensive surgery for locoregional and metastatic disease, local ablative therapies for metastases, and palliative chemotherapy, targeted therapy, and immunotherapy. Although these new treatment options have doubled overall survival for advanced disease to 3 years, survival is still best for those with non-metastasised disease. As the disease only becomes symptomatic at an advanced stage, worldwide organised screening programmes are being implemented, which aim to increase early detection and reduce morbidity and mortality from colorectal cancer.
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              A framework for advancing our understanding of cancer-associated fibroblasts

              Cancer-associated fibroblasts (CAFs) are a key component of the tumour microenvironment with diverse functions, including matrix deposition and remodelling, extensive reciprocal signalling interactions with cancer cells and crosstalk with infiltrating leukocytes. As such, they are a potential target for optimizing therapeutic strategies against cancer. However, many challenges are present in ongoing attempts to modulate CAFs for therapeutic benefit. These include limitations in our understanding of the origin of CAFs and heterogeneity in CAF function, with it being desirable to retain some antitumorigenic functions. On the basis of a meeting of experts in the field of CAF biology, we summarize in this Consensus Statement our current knowledge and present a framework for advancing our understanding of this critical cell type within the tumour microenvironment.
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                Author and article information

                Contributors
                chengquan@csu.edu.cn
                luopeng@smu.edu.cn
                304678@hospital.cqmu.edu.cn
                Journal
                Mol Cancer
                Mol Cancer
                Molecular Cancer
                BioMed Central (London )
                1476-4598
                2 October 2023
                2 October 2023
                2023
                : 22
                : 159
                Affiliations
                [1 ]Department of Neurosurgery, The Second Affiliated Hospital, Chongqing Medical University, ( https://ror.org/017z00e58) Chongqing, China
                [2 ]Department of Urology, The Second Affiliated Hospital, Chongqing Medical University, ( https://ror.org/017z00e58) Chongqing, China
                [3 ]Department of Neurosurgery, Central Hospital of Zhuzhou, ( https://ror.org/03prq2784) Zhuzhou, China
                [4 ]GRID grid.452223.0, ISNI 0000 0004 1757 7615, Department of Oncology, , Xiangya Hospital, Central South University, ; Changsha, China
                [5 ]College of Life Science and Technology, Huazhong University of Science and Technology, ( https://ror.org/00p991c53) Wuhan, China
                [6 ]Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, ( https://ror.org/056swr059) Zhengzhou, China
                [7 ]Department of Laboratory Medicine, The Second Affiliated Hospital, Chongqing Medical University, ( https://ror.org/017z00e58) Chongqing, China
                [8 ]GRID grid.452223.0, ISNI 0000 0004 1757 7615, Department of Neurosurgery, , Xiangya Hospital, Central South University, ; Changsha, China
                [9 ]GRID grid.452223.0, ISNI 0000 0004 1757 7615, National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, ; Changsha, China
                [10 ]GRID grid.417404.2, ISNI 0000 0004 1771 3058, Department of Oncology, , Zhujiang Hospital, Southern Medical University, ; Guangzhou, China
                Article
                1860
                10.1186/s12943-023-01860-5
                10544417
                37784082
                b03d5787-d1fe-48be-9d07-38a38656225a
                © BioMed Central Ltd., part of Springer Nature 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 19 June 2023
                : 13 September 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 82303610
                Award ID: 82372943
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002858, China Postdoctoral Science Foundation;
                Award ID: 2023MD734131
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100012546, Chongqing Postdoctoral Science Foundation;
                Award ID: CSTB2023NSCQBHX0002
                Award Recipient :
                Funded by: National Nature Science Foundation of China
                Award ID: 82073893
                Award Recipient :
                Funded by: Hunan Provincial Natural Science Foundation of China
                Award ID: NO.2022JJ20095
                Award Recipient :
                Funded by: Hunan Provincial Health Committee Foundation of China
                Award ID: NO.202204044869
                Award Recipient :
                Funded by: High level Medical Reserved Personnel Training Project of Chongqing. Kuanren Talents Program of the second affiliated hospital of Chongqing Medical University and Chongqing Scientific and Health Joint Medical Research Project
                Award ID: 2020GDRC021
                Award Recipient :
                Funded by: Cerebrovascular Disease Youth Innovation Fund by China International Medical Foundation
                Award ID: Z-2016-20-2201
                Award Recipient :
                Categories
                Review
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2023

                Oncology & Radiotherapy
                caf,clinical trial,microenvironment,immunotherapy,target
                Oncology & Radiotherapy
                caf, clinical trial, microenvironment, immunotherapy, target

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