The MYB-related transcription factor MYPOP acts as a selective regulator of cancer cell growth

Abstract The MYB-related transcription factor and partner of profilin (MYPOP or p42POP) is a ubiquitously expressed yet understudied protein recently identified as a restriction factor of oncogenic human papillomaviruses (HPV) and proposed tumor suppressor. Here we show that in HPV-transformed cervical cancer cells, MYPOP induces alterations in cell morphology, silences viral and cellular oncogenes including E6 and MYC , and stimulates the release of the cancer-killing cytokine interleukin-24. Transcriptomic and live-cell analyses reveal a rapid G1/S-phase arrest followed by loss of viable cervical cancer cells and induction of apoptosis. Moreover, MYPOP expression is broadly diminished across multiple human cancers, and its re-expression by both DNA- and mRNA-gene transfer markedly suppresses tumor cell proliferation while sparing normal epidermal keratinocytes. Similarly, murine Mypop inhibits mouse cancer cell growth. Collectively, our findings identify MYPOP as a selective suppressor of tumor cell proliferation across species in vitro and point to its potential relevance for future therapeutic investigation.

Authors

Publication Details

Journal
Communications Biology
Published
2026-05-19
DOI
https://doi.org/10.1038/s42003-026-10272-2
Primary Topic
Cervical Cancer and HPV Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The MYB-related transcription factor MYPOP acts as a selective regulator of cancer cell growth

Carina Osterhof, Thomas Hankeln, Sebastian Kreiter, Snježana Mikuličić et al.
Communications Biology
Cervical Cancer and HPV Research
article

The MYB-related transcription factor MYPOP acts as a selective regulator of cancer cell growth

Carina Osterhof, Thomas Hankeln, Sebastian Kreiter, Snježana Mikuličić, Barbara Schrörs, Matthias Plath, Tobias Bopp, Krishnaraj Rajalingam, Sascha Wagner, Mario Perković, Johannes Strunk, Luise Florin, Mustafa Diken, Tatjana Döring, M Suchan, Fédérico Marini, Matthias Klein, Andrea Nubbemeyer, Alena Hüppner, Mahwish Sial, Alina Henrich, Kirsten Freitag, Anne Kölsch, Marc A. Schneider, Gregory Harms, Annekathrin S. Nedwed, Silke Brill, Mika B. Sheriff
article en

Abstract

Abstract The MYB-related transcription factor and partner of profilin (MYPOP or p42POP) is a ubiquitously expressed yet understudied protein recently identified as a restriction factor of oncogenic human papillomaviruses (HPV) and proposed tumor suppressor. Here we show that in HPV-transformed cervical cancer cells, MYPOP induces alterations in cell morphology, silences viral and cellular oncogenes including E6 and MYC , and stimulates the release of the cancer-killing cytokine interleukin-24. Transcriptomic and live-cell analyses reveal a rapid G1/S-phase arrest followed by loss of viable cervical cancer cells and induction of apoptosis. Moreover, MYPOP expression is broadly diminished across multiple human cancers, and its re-expression by both DNA- and mRNA-gene transfer markedly suppresses tumor cell proliferation while sparing normal epidermal keratinocytes. Similarly, murine Mypop inhibits mouse cancer cell growth. Collectively, our findings identify MYPOP as a selective suppressor of tumor cell proliferation across species in vitro and point to its potential relevance for future therapeutic investigation.

Communications BiologyVol. 9(1)
Openalex Percentile: Top 4%
Cervical Cancer and HPV Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.