Current Advancements of Plant-Derived Agents for Triple-Negative Breast Cancer Therapy through Deregulating Cancer Cell Functions and Reprogramming Tumor Microenvironment.
Tai-Na WuHui-Ming ChenLie-Fen ShyurPublished in: International journal of molecular sciences (2021)
Triple-negative breast cancer (TNBC) is defined based on the absence of estrogen, progesterone, and human epidermal growth factor receptor 2 receptors. Currently, chemotherapy is the major therapeutic approach for TNBC patients; however, poor prognosis after a standard chemotherapy regimen is still commonplace due to drug resistance. Abnormal tumor metabolism and infiltrated immune or stromal cells in the tumor microenvironment (TME) may orchestrate mammary tumor growth and metastasis or give rise to new subsets of cancer cells resistant to drug treatment. The immunosuppressive mechanisms established in the TME make cancer cell clones invulnerable to immune recognition and killing, and turn immune cells into tumor-supporting cells, hence allowing cancer growth and dissemination. Phytochemicals with the potential to change the tumor metabolism or reprogram the TME may provide opportunities to suppress cancer metastasis and/or overcome chemoresistance. Furthermore, phytochemical intervention that reprograms the TME away from favoring immunoevasion and instead towards immunosurveillance may prevent TNBC metastasis and help improve the efficacy of combination therapies as phyto-adjuvants to combat drug-resistant TNBC. In this review, we summarize current findings on selected bioactive plant-derived natural products in preclinical mouse models and/or clinical trials with focus on their immunomodulatory mechanisms in the TME and their roles in regulating tumor metabolism for TNBC prevention or therapy.
Keyphrases
- drug resistant
- poor prognosis
- epidermal growth factor receptor
- clinical trial
- cancer therapy
- randomized controlled trial
- endothelial cells
- long non coding rna
- end stage renal disease
- stem cells
- advanced non small cell lung cancer
- squamous cell carcinoma
- drug delivery
- tyrosine kinase
- cystic fibrosis
- acinetobacter baumannii
- chronic kidney disease
- squamous cell
- induced apoptosis
- quantum dots
- endoplasmic reticulum stress
- prognostic factors
- single molecule
- sensitive detection
- estrogen receptor
- tissue engineering
- phase ii
- patient reported outcomes
- cell wall
- living cells
- patient reported