Beyond the Gut: The intratumoral microbiome's influence on tumorigenesis and treatment response.
Hao ZhangLi FuXinwen LeiliangChunrun QuWantao WuRong WenNing HuangQiuguang HeQuan ChenGuodong LiuYuan ChengPublished in: Cancer communications (London, England) (2024)
The intratumoral microbiome (TM) refers to the microorganisms in the tumor tissues, including bacteria, fungi, viruses, and so on, and is distinct from the gut microbiome and circulating microbiota. TM is strongly associated with tumorigenesis, progression, metastasis, and response to therapy. This paper highlights the current status of TM. Tract sources, adjacent normal tissue, circulatory system, and concomitant tumor co-metastasis are the main origin of TM. The advanced techniques in TM analysis are comprehensively summarized. Besides, TM is involved in tumor progression through several mechanisms, including DNA damage, activation of oncogenic signaling pathways (phosphoinositide 3-kinase [PI3K], signal transducer and activator of transcription [STAT], WNT/β-catenin, and extracellular regulated protein kinases [ERK]), influence of cytokines and induce inflammatory responses, and interaction with the tumor microenvironment (anti-tumor immunity, pro-tumor immunity, and microbial-derived metabolites). Moreover, promising directions of TM in tumor therapy include immunotherapy, chemotherapy, radiotherapy, the application of probiotics/prebiotics/synbiotics, fecal microbiome transplantation, engineered microbiota, phage therapy, and oncolytic virus therapy. The inherent challenges of clinical application are also summarized. This review provides a comprehensive landscape for analyzing TM, especially the TM-related mechanisms and TM-based treatment in cancer.
Keyphrases
- dna damage
- cell proliferation
- signaling pathway
- current status
- gene expression
- stem cells
- early stage
- radiation therapy
- epithelial mesenchymal transition
- pi k akt
- immune response
- ms ms
- poor prognosis
- squamous cell carcinoma
- microbial community
- locally advanced
- toll like receptor
- bone marrow
- small molecule
- cystic fibrosis
- long non coding rna
- papillary thyroid
- endoplasmic reticulum stress
- replacement therapy