Table 1

The influence of microbes on cancer development

MalignancyMethodsMain resultsReferences
Head and neck cancerMeta-analysisOral microbiota converts alcohol into acetaldehyde, thus causing cancer.26
Case-control studyHPV is widely considered an independent risk factor inducing OPSCC.30
Murine modelP. gingivalis and F. nucleatum infection promotes OSCC via the IL-6-STAT3 pathway.33
Case-control studyP. melaninogenica, C. gingivalis, and S. mitis are elevated in the saliva of individuals with OSCC.34
Case-control studyActinomyces and Firmicutes are significantly depleted in tumor tissue relative to normal tissue.35
Colorectal cancer (CRC)Case-control studyFusobacterium and Porphyromonas are detectable in samples from patients with CRC.40
Case-control studyTreponema denticola and Prevotella intermedia are associated with increased risk of CRC.41
Murine modelF. nucleatum precipitates CRC carcinogenesis via immune modulation, virulence factors, microRNAs, and bacterial metabolism.44
Case-control studyGemella, Peptostreptococcus, and Parvimonas are found in CRC.40
Case-control studyGut microbial dysbiosis contributes to the development of CRC.61
Case-control studyLower relative abundance of Clostridia and higher relative abundance of Porphyromonas and Fusobacterium are found in patients with CRC.42
Murine modelStool microbiota from patients with CRC promotes colorectal carcinogenesis in mice.63
Case-control studyStreptococcus bovis is a risk factor for colonic tumors.66
Murine modelETBF is highly expressed in patients with CRC compared with healthy people.67,68
Murine modelE. coli induces tumorigenesis through generating DNA mutagens.70
Murine modelCampylobacter jejuni promotes CRC through the genotoxic action of cytolethal distending toxin.71
Pancreatic cancerCase-control studyThe Bacteroides genus and Granulicatella adiacens are more common in patients with pancreatic cancer than healthy people; however, Neisseria elongata and Streptococcus mitis are present in lower concentrations in pancreatic cancer.49
Case-control studyP. gingivalis may contribute to a higher risk of pancreatic cancer.51
Case-control studyAggregatibacter actinomycetemcomitans and P. gingivalis in the oral cavity are associated with pancreatic carcinogenesis, whereas the phylum Fusobacteria and its genus Leptotrichia are protective and decrease the risk.13
Liver cancerMurine modelGut bacterial metabolites cause DNA damage and carcinogenesis.79
Murine modelGut bacteria-controlled bile acids may alter immune function, thus influencing tumor growth.81
Murine modelIntestinal microbiota and lipopolysaccharide accelerate hepatocarcinogenesis.82
Murine modelA gram-positive gut microbial component increases the risk of cancer development through creating a tumor-promoting microenvironment.83
Breast cancerCase-control studyThe intestinal flora in patients with breast cancer is different from that in healthy controls.85
Murine modelGut dysbiosis affects mammary tumor dissemination.88