Fibroblast stromal support model for predicting human papillomavirus-associated cancer drug responses

Human papillomavirus-related cancers (HPV<sup>+</sup> cancers) remain a significant public health concern, and specific clinical approaches are desperately needed. In translating drug response data from <i>in vitro</i> to <i>in vivo</i>, the fibroblasts of the adjacent stromal support network play a key role. Our study presents the utilization of a fibroblast 2D co-culture system to better predict translational drug assessments for HPV<sup>+</sup> cancers. We also suggest that this co-culture system should be considered for other translational approaches. Predicting even a portion of treatment paradigms that may fail <i>in vivo</i> with a co-culture model will yield significant time, effort, resource, and cost efficiencies.

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Publication Details

Journal
Journal of Virology
Published
2024-09-13
DOI
https://doi.org/10.1128/jvi.01024-24
Citations
1
Primary Topic
Head and Neck Cancer Studies
Type
article
Field-Weighted Citation Impact
0.58

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article

Fibroblast stromal support model for predicting human papillomavirus-associated cancer drug responses

Molly L. Bristol, Rachel L. Lewis, Raymonde Otoa, Claire D. James et al.
1 citations
Journal of Virology
Head and Neck Cancer Studies
0.58
article

Fibroblast stromal support model for predicting human papillomavirus-associated cancer drug responses

Molly L. Bristol, Rachel L. Lewis, Raymonde Otoa, Claire D. James, Apurva T. Prabhakar, Alexis L. Fakunmoju, Nabiha M. Rais, Xu Wang, Aya H. Youssef, J. Mathew Machado, Austin J. Witt
article en
1 citations

Abstract

Human papillomavirus-related cancers (HPV<sup>+</sup> cancers) remain a significant public health concern, and specific clinical approaches are desperately needed. In translating drug response data from <i>in vitro</i> to <i>in vivo</i>, the fibroblasts of the adjacent stromal support network play a key role. Our study presents the utilization of a fibroblast 2D co-culture system to better predict translational drug assessments for HPV<sup>+</sup> cancers. We also suggest that this co-culture system should be considered for other translational approaches. Predicting even a portion of treatment paradigms that may fail <i>in vivo</i> with a co-culture model will yield significant time, effort, resource, and cost efficiencies.

Journal of VirologyVol. 98(10)
Virginia Commonwealth University (US), Virginia Cancer Institute (US), VCU Massey Comprehensive Cancer Center (US)
U.S. Department of Health and Human Services, Virginia Commonwealth University, National Institutes of Health, National Cancer Institute, National Institute of Dental and Craniofacial Research
Good health and well-being
Openalex Percentile: Top 31%
Head and Neck Cancer Studies
0.58
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