The updated landscape of tumor microenvironment and drug repurposing.
Ming-Zhu JinWei-Lin JinPublished in: Signal transduction and targeted therapy (2020)
Accumulating evidence shows that cellular and acellular components in tumor microenvironment (TME) can reprogram tumor initiation, growth, invasion, metastasis, and response to therapies. Cancer research and treatment have switched from a cancer-centric model to a TME-centric one, considering the increasing significance of TME in cancer biology. Nonetheless, the clinical efficacy of therapeutic strategies targeting TME, especially the specific cells or pathways of TME, remains unsatisfactory. Classifying the chemopathological characteristics of TME and crosstalk among one another can greatly benefit further studies exploring effective treating methods. Herein, we present an updated image of TME with emphasis on hypoxic niche, immune microenvironment, metabolism microenvironment, acidic niche, innervated niche, and mechanical microenvironment. We then summarize conventional drugs including aspirin, celecoxib, β-adrenergic antagonist, metformin, and statin in new antitumor application. These drugs are considered as viable candidates for combination therapy due to their antitumor activity and extensive use in clinical practice. We also provide our outlook on directions and potential applications of TME theory. This review depicts a comprehensive and vivid landscape of TME from biology to treatment.
Keyphrases
- combination therapy
- papillary thyroid
- stem cells
- squamous cell
- clinical practice
- low dose
- squamous cell carcinoma
- young adults
- climate change
- coronary artery disease
- risk assessment
- oxidative stress
- cancer therapy
- lymph node metastasis
- cell proliferation
- signaling pathway
- acute coronary syndrome
- cardiovascular events
- percutaneous coronary intervention
- pi k akt
- drug induced
- endoplasmic reticulum stress