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      The role of Hedgehog and Notch signaling pathway in cancer

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          Abstract

          Notch and Hedgehog signaling are involved in cancer biology and pathology, including the maintenance of tumor cell proliferation, cancer stem-like cells, and the tumor microenvironment. Given the complexity of Notch signaling in tumors, its role as both a tumor promoter and suppressor, and the crosstalk between pathways, the goal of developing clinically safe, effective, tumor-specific Notch-targeted drugs has remained intractable. Drugs developed against the Hedgehog signaling pathway have affirmed definitive therapeutic effects in basal cell carcinoma; however, in some contexts, the challenges of tumor resistance and recurrence leap to the forefront. The efficacy is very limited for other tumor types. In recent years, we have witnessed an exponential increase in the investigation and recognition of the critical roles of the Notch and Hedgehog signaling pathways in cancers, and the crosstalk between these pathways has vast space and value to explore. A series of clinical trials targeting signaling have been launched continually. In this review, we introduce current advances in the understanding of Notch and Hedgehog signaling and the crosstalk between pathways in specific tumor cell populations and microenvironments. Moreover, we also discuss the potential of targeting Notch and Hedgehog for cancer therapy, intending to promote the leap from bench to bedside.

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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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            The canonical Notch signaling pathway: unfolding the activation mechanism.

            Notch signaling regulates many aspects of metazoan development and tissue renewal. Accordingly, the misregulation or loss of Notch signaling underlies a wide range of human disorders, from developmental syndromes to adult-onset diseases and cancer. Notch signaling is remarkably robust in most tissues even though each Notch molecule is irreversibly activated by proteolysis and signals only once without amplification by secondary messenger cascades. In this Review, we highlight recent studies in Notch signaling that reveal new molecular details about the regulation of ligand-mediated receptor activation, receptor proteolysis, and target selection.
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              EMT, CSCs, and drug resistance: the mechanistic link and clinical implications

              According to the cancer stem cell (CSC) paradigm, a minor subpopulation of cancer cells with stem-cell properties predominantly underlies tumour progression, therapy resistance, and disease recurrence. Notably, epithelial-to-mesenchymal transition (EMT) is implicated in these processes, and CSCs typically show markers of EMT-programme activation. Herein, the authors outline our current understanding of the links between the EMT programme, the CSC phenotype, metastasis, and drug resistance, and discuss the potential for therapeutic targeting of these facets of tumour biology.
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                Author and article information

                Contributors
                yangjing1@sysucc.org.cn
                drmaxuelei@gmail.com
                Journal
                Mol Biomed
                Mol Biomed
                Molecular Biomedicine
                Springer Nature Singapore (Singapore )
                2662-8651
                15 December 2022
                15 December 2022
                December 2022
                : 3
                : 44
                Affiliations
                [1 ]GRID grid.13291.38, ISNI 0000 0001 0807 1581, Department of Biotherapy, , West China Hospital and State Key Laboratory of Biotherapy, Sichuan University, ; 37 Guoxue Xiang Street, Chengdu, 610041 Sichuan Province China
                [2 ]GRID grid.13291.38, ISNI 0000 0001 0807 1581, West China School of Medicine, , Sichuan University, ; Chengdu, China
                [3 ]GRID grid.488530.2, ISNI 0000 0004 1803 6191, Melanoma and Sarcoma Medical Oncology Unit, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, , Sun Yat-Sen University Cancer Center, ; 651 Dongfeng Road East, Guangzhou, 510060 China
                [4 ]GRID grid.488530.2, ISNI 0000 0004 1803 6191, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, , Sun Yat-Sen University Cancer Center, ; Guangzhou, 510060 P. R. China
                Author information
                http://orcid.org/0000-0002-9148-5001
                Article
                99
                10.1186/s43556-022-00099-8
                9751255
                36517618
                b78169f0-126b-40db-abc1-8c3a0a6c518a
                © The Author(s) 2022

                Open AccessThis 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/.

                History
                : 5 September 2022
                : 25 October 2022
                Categories
                Review
                Custom metadata
                © The Author(s) 2022

                notch,hedgehog,cancer,cancer stem cell,tumor microenvironment

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