Review Article

The Cancer Microbiota: EMT and Inflammation as Shared Molecular Mechanisms Associated with Plasticity and Progression

Table 1

Main identified/studied bacterial phyla and their relationship with carcinogenesis.

Bacterial PhylumBody siteDetrimental/beneficial for the hostReference

ActinobacteriaColonBeneficial (though outcompeted by opportunistic bacteria during cancer progression)[95, 97]
EsophagusBeneficial[68, 69]

BacteroidetesColonDetrimental, linked to development of CRC[95, 97]
EsophagusDetrimental, linked to development of esophageal cancer[57, 68, 69]
Female reproductive tractDetrimental, linked to endometrial cancer[118]
Oral cavityDetrimental, related to development of OSCC[18ā€“20]

FirmicutesBreastStaphylococcus: detrimental, linked to development of breast cancer
Lactobacillus: beneficial
[37, 43]
ColonBeneficial (though outcompeted by opportunistic bacteria during cancer progression)[95, 97]
EsophagusDetrimental, linked to development of esophageal cancer
Peptococcus: beneficial
[57, 68, 69]
Female reproductive tractDetrimental, linked to ovarian cancer
Lactobacillus: beneficial
[119, 124, 125]
Nasal cavityDetrimental, related to development of nasal polyposis[28, 29]
SkinDetrimental, linked to atopic dermatitis and BCC (S. aureus) or beneficial (S. epidermidis)[131, 135]

FusobacteriaColonDetrimental, linked to development of CRC[86, 110ā€“112]
EsophagusDetrimental, linked to development of esophageal cancer[57]
Oral cavityDetrimental, related to development of OSCC[16, 17]

ProteobacteriaBreastDetrimental, linked to development of breast cancer[37]
EsophagusDetrimental, linked to development of esophageal cancer[53, 57, 75]
Female reproductive tractDetrimental, linked to ovarian cancer[124, 125]