Role of tumor microenvironment in cancer progression and therapeutic strategy.
Qingjing WangXueting ShaoYuxuan ZhangMiaojin ZhuFrederick X C WangJianjian MuJiaxuan LiHang-Ping YaoKeda ChenPublished in: Cancer medicine (2023)
Cancer is now considered a tumor microenvironment (TME) disease, although it was originally thought to be a cell and gene expression disorder. Over the past 20 years, significant advances have been made in understanding the complexity of the TME and its impact on responses to various anticancer therapies, including immunotherapies. Cancer immunotherapy can recognize and kill cancer cells by regulating the body's immune system. It has achieved good therapeutic effects in various solid tumors and hematological malignancies. Recently, blocking of programmed death-1 (PD-1), programmed death-1 ligand-1 (PD-L1), and programmed death Ligand-2 (PD-L2), the construction of antigen chimeric T cells (CAR-T) and tumor vaccines have become popular immunotherapies Tumorigenesis, progression, and metastasis are closely related to TME. Therefore, we review the characteristics of various cells and molecules in the TME, the interaction between PD-1 and TME, and promising cancer immunotherapy therapeutics.
Keyphrases
- gene expression
- papillary thyroid
- cell therapy
- squamous cell
- induced apoptosis
- dna methylation
- single cell
- small molecule
- cell cycle arrest
- stem cells
- lymph node metastasis
- signaling pathway
- oxidative stress
- bone marrow
- cell proliferation
- childhood cancer
- young adults
- endoplasmic reticulum stress
- cell death
- drug induced