Evidence map›Paper›PMID 42702935›Full record

ArticleCancer medicine2026

STK11 Mutations and Deletions Define an Aggressive Molecular Subgroup of Cervical Adenocarcinoma.

Emma W Robinson, Elisabeth A Murphy, Anaseidy Albanez, Sonam Tulsyan, Hong Lou, Yi Xie, Weiyin Zhou, Qian Yang, Tawnjerae Joe, Tongwu Zhang and 13 more

Abstract read
In one paragraph

Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

  • Update of
    2026
5 · Who and what money

Authors and funding

23 authors.

Emma W RobinsonDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.
Elisabeth A MurphyCaris Life Sciences, Irving, Texas, USA.
Anaseidy AlbanezInstituto de Cancerología (INCAN), Guatemala City, Guatemala.
Sonam TulsyanDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.ORCID https://orcid.org/0000-0001-7201-571X
Hong LouCancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research, Rockville, Maryland, USA.
Yi XieDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.ORCID https://orcid.org/0000-0003-2150-8973
Weiyin ZhouCancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research, Rockville, Maryland, USA.ORCID https://orcid.org/0000-0002-0467-3064
Qian YangDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.
Tawnjerae JoeDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.
Tongwu ZhangDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.
Jia LiuCancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research, Rockville, Maryland, USA.
Wen LuoCancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research, Rockville, Maryland, USA.
Dongjing WuCancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research, Rockville, Maryland, USA.
Herbert HigsonCancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research, Rockville, Maryland, USA.
Mathias ViardBasic Science Program, Frederick National Laboratory for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.
Mary CarringtonBasic Science Program, Frederick National Laboratory for Cancer Research, National Cancer Institute, Frederick, Maryland, USA.ORCID https://orcid.org/0000-0002-2692-2180
Matthew OberleyCaris Life Sciences, Irving, Texas, USA.
Hesler MoralesInstituto de Cancerología (INCAN), Guatemala City, Guatemala.
Lisa MirabelloDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.
Enrique AlvirezHospital Central Universitario "Dr. Antonio M Pineda", Barquisimeto, Lara State, Venezuela.
Roberto OrozcoHospital General San Juan de Dios, Guatemala City, Guatemala.ORCID https://orcid.org/0000-0002-3785-2827
Eduardo GharzouziIntegra Cancer Center, Guatemala City, Guatemala.
Michael DeanDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, Maryland, USA.ORCID https://orcid.org/0000-0003-2234-0631

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI PENDLETON, RICHARD · 2019 to 2025
$3932.6M
NCI NIH HHS 75N91019D00024NIH HHS 75N91019D00024
6 · The paper itself

Abstract

Cervical adenocarcinoma accounts for 15%-20% of cervical cancers and is associated with poorer survival and reduced response to screening and immunotherapy compared with squamous cell carcinoma (SCC). The genomic drivers underlying this molecular subgroup remain incompletely characterized. Whole-exome sequencing was performed on 302 invasive cervical cancers from Guatemala and Venezuela. Structural variation analysis was conducted using SNP-array and whole-genome sequencing data. Findings were replicated in more than 4600 additional cervical cancer samples from TCGA, AACR Project GENIE, MSKCC, and Caris datasets. TP53 mutations were more frequent in adenocarcinoma than SCC, particularly in HPV-negative tumors. STK11 alterations, including mutations and focal deletions, were significantly enriched in HPV-positive adenocarcinomas compared with SCC and affected 23% of adenocarcinomas overall. Whole-genome analyses identified recurrent focal deletions, inversions, chromosomal rearrangements, and breakage-fusion-bridge events involving chromosome 19p and STK11 that were not detected by exome sequencing alone. STK11 alterations were associated with younger age at diagnosis, poorer overall survival, and inferior outcomes following immune checkpoint inhibitor (ICI) therapy. STK11 alterations significantly co-occurred with YAP1 amplification but were largely mutually exclusive with PIK3CA mutation. Cervical adenocarcinomas also demonstrated significantly lower CD274 (PD-L1) expression than SCC. STK11 alterations define a distinct molecular subgroup of cervical adenocarcinoma characterized by structural disruption of chromosome 19p, younger age at onset, and poorer clinical outcomes. These findings have implications for molecular classification and future targeted therapeutic approaches in cervical cancer.

Indexed as

AdenocarcinomaMutationProtein Serine-Threonine KinasesUterine Cervical NeoplasmsAMP-Activated Protein Kinase KinasesBiomarkers, TumorExome SequencingFemaleHumansMiddle AgedAMP-Activated Protein Kinase KinasesBiomarkers, TumorProtein Serine-Threonine KinasesSTK11 protein, humanadenocarcinomacervical cancerhuman papillomavirusSTK11 tumor suppressorwhole exome sequencing

Identifiers

PMID42702935
PMCPMC13547848

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.