Evidence map›Paper›PMID 42039303›Full record

ArticleFrontiers in transplantation2026

Cell cycle pathway alterations predict outcomes post-liver transplantation for hepatocellular carcinoma.

Ashton A Connor, Mahinur Mattohti, Sudha Kodali, Maen Abdelrahim, Ahmed Elaileh, Samar Semaan, Youssef Dib, Khush Patel, Jason Todd, Urmi Sengupta and 17 more

Abstract read
In one paragraph

Article in Frontiers in transplantation, 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

27 authors.

Ashton A ConnorDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Mahinur MattohtiImmunobiology and Transplant Science Center, Houston Methodist Research Institute, Houston Methodist Hospital, Houston, TX, United States.
Sudha KodaliJC Walter Jr Transplant Center, Houston Methodist Hospital, Houston, TX, United States.
Maen AbdelrahimDepartment of Medicine, Weill Cornell Medical College, New York, NY, United States.
Ahmed ElailehDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Samar SemaanDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Youssef DibDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Khush PatelDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Jason ToddDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Urmi SenguptaDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Constance M MobleyDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Caroline J SimonDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Yee Lee CheahDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Ashish SahariaDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Mary R SchwartzCockrell Center Phase 1 Unit, Cockrell Center for Advanced Therapeutics, Houston Methodist Hospital, Houston, TX, United States.
Sadhna DhingraCockrell Center Phase 1 Unit, Cockrell Center for Advanced Therapeutics, Houston Methodist Hospital, Houston, TX, United States.
Jessica S ThomasCockrell Center Phase 1 Unit, Cockrell Center for Advanced Therapeutics, Houston Methodist Hospital, Houston, TX, United States.
Randall J OlsenCockrell Center Phase 1 Unit, Cockrell Center for Advanced Therapeutics, Houston Methodist Hospital, Houston, TX, United States.
Linda W MooreDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Kirk HeyneDepartment of Medicine, Weill Cornell Medical College, New York, NY, United States.
Xian C LiJC Walter Jr Transplant Center, Houston Methodist Hospital, Houston, TX, United States.
David W VictorJC Walter Jr Transplant Center, Houston Methodist Hospital, Houston, TX, United States.
Timothy E NewhookThe University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Ahmed O KasebThe University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Jean-Nicolas VautheyThe University of Texas MD Anderson Cancer Center, Houston, TX, United States.
A Osama GaberDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
R Mark GhobrialDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatocellular carcinoma (HCC) incidence and mortality are rising. Liver transplantation (LT) offers the best outcomes, but current tumor size- and number-based selection criteria restrict access. Molecular profiling may better reflect tumor biology and guide precision-based selection strategies. Methods: This prospective single-center study included patients with HCC who had undergone LT between 11 November 2016 and 4 April 2023 with sufficient tumor cellularity in explanted livers. Tumor DNA was subjected to targeted sequencing for 38 genes, with the results returned to clinicians. Altered genes were grouped into HCC-relevant signaling pathways. Outcomes included post-LT overall survival (OS), recurrence-free survival (RFS), and recurrence sites. The Cancer Genome Atlas (TCGA) HCC cohort was used for validation. Results: Among 1,103 LT recipients, 261 were for HCC and 91 underwent sequencing. Most patients were male ( Conclusion: Post-LT molecular profiling of HCC reveals tumor-specific alterations associated with outcomes, supporting the incorporation of tumor biology into future LT selection criteria.

Indexed as

biomarkerscell cycle pathwayhepatocellular carcinomaliver transplantationmolecular profiling

Identifiers

PMID42039303
PMCPMC13106343

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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.