@article{632f3114775d41d6a077a455c5a813ac,
title = "Porphyromonas somerae Invasion of Endometrial Cancer Cells",
abstract = "Recent evidence suggests an association between endometrial cancer and the understudied bacterial species Porphyromonas somerae. This association was demonstrated in previous work that indicated a significantly enriched abundance of P. somerae in the uterine microbiome of endometrial cancer patients. Given the known associations of the Porphyromonas genus and oral cancer, we hypothesized that P. somerae may play a similar pathogenic role in endometrial cancer via intracellular activity. Before testing our hypothesis, we first characterized P. somerae biology, as current background data is limited. These novel characterizations include growth curves in liquid medium and susceptibility tests to antibiotics. We tested our hypothesis by examining growth changes in response to 17β-estradiol, a known risk factor for endometrial cancer, followed by metabolomic profiling in the presence and absence of 17β-estradiol. We found that P. somerae exhibits increased growth in the presence of 17β-estradiol of various concentrations. However, we did not find significant changes in metabolite levels in response to 17β-estradiol. To study direct host-microbe interactions, we used in vitro invasion assays under hypoxic conditions and found evidence for intracellular invasion of P. somerae in endometrial adenocarcinoma cells. We also examined these interactions in the presence of 17β-estradiol but did not observe changes in invasion frequency. Invasion was shown using three lines of evidence including visualization via differential staining and brightfield microscopy, increased frequency of bacterial recovery after co-culturing, and in silico methods to detail relevant genomic and transcriptomic components. These results underscore potential intracellular phenotypes of P. somerae within the uterine microbiome. Furthermore, these results raise new questions pertaining to the role of P. somerae in the progression of endometrial cancer.",
keywords = "Porphyromonas somerae, endometrial cancer, estradiol, fumarate reductase, intracellular invasion, metabolomics, succinate dehydrogenase",
author = "Crooks, {Taylor A.} and Madison, {Joseph D.} and Walsh, {Dana M.} and Herbert, {William G.} and Jeraldo, {Patricio R.} and Nicholas Chia and Cliby, {William A.} and Kaufmann, {Scott H.} and Walther-Antonio, {Marina R.S.}",
note = "Funding Information: We would like to thank the members of the Chia, Kashyap, and Walther-Antonio lab for their support with special thanks to Janet Yao and Nancy Scott for their continuous assistance with cell and lab maintenance. We would also like to thank Talia Wiggen, Leslie Kent, and the Hunter lab for their advice and support during the manuscript writing process, Stephanie Song for her help and support during the tumultuous times of the COVID-19 pandemic, Samantha Shannon for her advice and insight in Porphyromonas culturing techniques on blood agar, and Meng Pu for her assistance in image processing. Finally, we would like to offer our thanks to Err and Ignignokt Mooninite for their assistance and motivation during the long hours of our invasion assays. Funding. This project was supported by CTSA Grant No. KL2TR002379 from the National Center for Advancing Translational Science (NCATS). This work was also supported, in part, by a career enhancement award from NIH grants P50CA136393, U24DK100469, and UL1TR000135. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH. Part of the work by JM was completed while supported by the NSF Postdoctoral Research Fellowships in Biology Program under Grant No. 1907311. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation. Funding Information: This project was supported by CTSA Grant No. KL2TR002379 from the National Center for Advancing Translational Science (NCATS). This work was also supported, in part, by a career enhancement award from NIH grants P50CA136393, U24DK100469, and UL1TR000135. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH. Part of the work by JM was completed while supported by the NSF Postdoctoral Research Fellowships in Biology Program under Grant No. 1907311. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation. Publisher Copyright: {\textcopyright} Copyright {\textcopyright} 2021 Crooks, Madison, Walsh, Herbert, Jeraldo, Chia, Cliby, Kaufmann and Walther-Antonio.",
year = "2021",
month = jul,
day = "23",
doi = "10.3389/fmicb.2021.674835",
language = "English (US)",
volume = "12",
journal = "Frontiers in Microbiology",
issn = "1664-302X",
publisher = "Frontiers Media S. A.",
}