Fusobacteria modulate oral carcinogenesis and promote cancer progression.
Fusobacteria modulate oral carcinogenesis and promote cancer progression.
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梭菌调节口腔癌发生并促进癌症进展。
DOI:
10.1080/20002297.2020.1849493
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发表时间:
2020-11-30
影响因子:
4.5
通讯作者:
Chan EKL
中科院分区:
文献类型:
--
作者:
Harrandah AM;Chukkapalli SS;Bhattacharyya I;Progulske-Fox A;Chan EKL
Background: Evidence suggest periodontal bacterial infection can contribute to oral cancer initiation and progression. Aim: To investigate the effects of periodontal bacteria on oral cancer cell behavior using a cell-based system and a mouse carcinogenesis model. Methods: Oral cancer cell lines were polyinfected with four periodontal bacteria. Cytokine levels and relative changes in oncogene mRNA expression were determined post-infection. Oral tumours in mice induced by 4-nitroquinoline-1-oxide (4NQO) were compared with and without administrating periodontal bacteria. Results: Polyinfected oral cancer cells had upregulated MMP1, MMP9, and IL-8. The expression of cell survival markers MYC, JAK1, and STAT3 and epithelial-mesenchymal transition markers ZEB1 and TGF-β were also significantly elevated. Monoinfections showed F. nucleatum alone had comparable or greater effects than the four bacteria together. Fusobacterial culture supernatant, primarily LPS, was sufficient to induce IL-8 secretion, demonstrating that direct contact of live Fusobacteria with cancer cells might not be required to exert changes in cancer cell behaviour. In the 4NQO-induced oral tumour model, mice infected with bacteria developed significantly larger and more numerous lesions compared to those not infected. Conclusion: This study demonstrated that Fusobacteria could potentially enhance cancer cell invasiveness, survival, and EMT when presented in the oral tumour microenvironment. Abbreviations: 4NQO, 4-nitroquinoline-1-oxide; ELISA, enzyme-linked immunosorbent assay; EMT, epithelial–mesenchymal transition; IL-8, interleukin-8; JAK1, Janus kinase 1; LPS, lipopolysaccharide; MMP, matrix metalloproteinase; OSCCs, oral squamous cell carcinomas; PK, proteinase K; PMB, Polymyxin B; qRT-PCR, quantitative real-time polymerase chain reaction; STAT3, signal transducer and activator of transcription 3; TGF-β, transforming growth factor beta; ZEB1, zinc finger E-Box binding homeobox 1
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影响因子:
5.4
作者:
Han YW
通讯作者:
Han YW
影响因子:
--
作者:
Binder Gallimidi A;Fischman S;Revach B;Bulvik R;Maliutina A;Rubinstein AM;Nussbaum G;Elkin M
通讯作者:
Elkin M
DOI:
10.1002/hed.2880160506
发表时间:
1994-09-01
影响因子:
2.9
作者:
HAWKINS, BL;HENIFORD, BW;HENDLER, FJ
通讯作者:
HENDLER, FJ
影响因子:
7
作者:
Castellarin, Mauro;Warren, Rene L.;Holt, Robert A.
通讯作者:
Holt, Robert A.
影响因子:
4.8
作者:
Bremmer, Jantine F.;Brakenhoff, Ruud H.;Braakhuis, Boudewijn J. M.
通讯作者:
Braakhuis, Boudewijn J. M.