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ISSN 2472-0429

Advances in Cancer Prevention
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Understanding the Role of the Tumor Microenvironment in Bladder Cancer Progression

Giggle Ganja*
Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, U.S.A
*Corresponding Author: Giggle Ganja, Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, U.S.A, Email: giggle@gmail.com

Received Date: Sep 02, 2024 / Published Date: Sep 30, 2024

Citation: Giggle G (2024) Understanding the Role of the Tumor Microenvironment in Bladder Cancer Progression Adv Cancer Prev 8: 247.

Copyright: © 2024 Giggle G. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 
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Abstract

Bladder cancer progression is influenced not only by the genetic mutations within tumor cells but also by the dynamic interactions between the tumor and its surrounding microenvironment. The tumor microenvironment (TME) plays a critical role in regulating cancer growth, invasion, metastasis, and resistance to treatment. This review examines the components of the TME in bladder cancer, including immune cells, fibroblasts, extracellular matrix, and signaling molecules, and their contributions to tumor progression. Special attention is given to the immunosuppressive nature of the TME, which limits the effectiveness of immune-based therapies. Understanding the molecular crosstalk between tumor cells and the TME offers valuable insights into bladder cancer biology and presents new therapeutic opportunities. Targeting the TME, either alone or in combination with existing treatments, holds promise in overcoming treatment resistance and improving outcomes for bladder cancer patients. This paper highlights the emerging strategies aimed at modulating the TME and discusses the potential of these approaches in advancing bladder cancer treatment.

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Citations : 352

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  • OCLC- WorldCat
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