Author
Listed:
- Manoli
- Rampal
- Balaji
- Sadangi
- Singh
- Mahajan
Abstract
The tumor microenvironment (TME) is very important for how cancer starts, grows, and becomes resistant to treatment. It is made up of different kinds of cells, like cancer cells, immune cells, fibroblasts, vascular cells, and extracellular matrix (ECM) components. These cells interact with each other to make a complicated and changing environment that affects how the tumor behaves. Understanding the TME is important for making cancer treatments better because it helps us understand how immune systems hide cancer, how it spreads, and how drugs don't work on it. This abstract looks at ways to improve cancer treatment by learning more about the TME. One potential method is to target immune cells in the TME, like tumor-associated macrophages, regulatory T cells, and myeloid-derived suppressor cells, which often help the immune system tolerate the tumor and it grows. It is possible to recover immune function and make immunotherapies like immune checkpoint inhibitors work better by changing these groups of immune cells. Disrupting the ECM is another approach. The ECM not only supports the shape of the tumor but also controls cell communication and the growth of drug tolerance. To improve drug transport and stop tumor spread, scientists are looking into agents that target ECM components or enzymes that change it. The TME's blood vessels are another important part of how the growth grows. Problematic blood veins can make it harder for healing agents to get to where they need to go, which makes drugs less effective. Strategies like arterial normalization or using nanomedicine to target blood vessels that leak have shown promise in making it easier for drugs to get into cells and treatment to work better. Targeting the metabolic reprogramming of tumor cells and the TME's changed food supply can also make treatments more effective, especially when they are used with radiation or chemotherapy.
Suggested Citation
Handle:
RePEc:dbk:health:v:4:y:2025:i::p:430:id:430
DOI: 10.56294/hl2025430
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