Evidence map›Paper›PMID 42427638›Full record

ArticlebioRxiv : the preprint server for biology2026

Aging increases ovarian cancer growth, metastasis, and immunosuppression that can be alleviated by inhibiting hedgehog signaling.

Asha Kumari, Mohamed Halaby Elbahoty, Resha Rajkarnikar, Khushi Sureja, Manan Virendra Nayyar, Mehri Monavarian, Liz Macias Quintero, Katherine Fuh, Daniel J Tyrrell, Lalita A Shevde and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Asha KumariDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0002-2508-9879
Mohamed Halaby ElbahotyDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0001-8766-4616
Resha RajkarnikarDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0002-8724-0052
Khushi SurejaDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.
Manan Virendra NayyarDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.
Mehri MonavarianDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0002-3320-2974
Liz Macias QuinteroDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0001-7641-4582
Katherine FuhDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA.ORCID 0000-0002-7693-2694
Daniel J TyrrellDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0002-0811-6724
Lalita A ShevdeDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0002-1520-1476
Sudarshan AnandDepartment of Cell, Development and Cancer Biology, Department of Radiation Medicine and Knight Cancer Institute, Oregon Health & Science University, Portland, OR.ORCID 0000-0002-4969-6884
Camilla MargaroliDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0003-3952-0778
Karthikeyan MythreyeDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Heersink School of Medicine, Birmingham, Alabama, USA.ORCID 0000-0001-5478-0098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer incidence and mortality increase with age, yet how aging shapes tumor progression and the immune microenvironment remains poorly defined. Using orthotopic syngeneic models of distinct cellular origins (ovarian surface epithelial and fallopian tube-derived) in young versus aged mice, we show that aged hosts exhibit higher tumor burden, metastasis and ascites. Follicle depletion in young mice did not recapitulate these effects, indicating contributions beyond hormonal decline. Spatial transcriptomics revealed distinct age dependent intratumoral heterogeneity, with Hedgehog signaling enrichment in CD45

Indexed as

AgingHedgehogImmunosuppressionOvarian cancer

Identifiers

PMID42427638
PMCPMC13345016

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.