Evidence map›Paper›PMID 42372207›Full record

ArticleJCO precision oncology2026

Integrating DNA Mutations and RNA Expression of Cancer Driver Genes in Asian Rare Cancers: A Pan-Cancer Analysis.

Kathleen Yasmin de Almeida, Marcelo Severino B Imasa, Pei Jye Voon, Hwoei Fen Soo Hoo, Tom Wei-Wu Chen, Suhana Yusak, Rangasamy Ramachandran, Najihah Abu Bakar, Ming-Huang Chen, Yasushi Yatabe and 3 more

Abstract read
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Article in JCO precision oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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.

Kathleen Yasmin de AlmeidaDepartment of International Clinical Development, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-8568-7897
Marcelo Severino B ImasaDepartment of Internal Medicine, St Luke's Medical Center, Quezon, Philippines.
Pei Jye VoonDepartment of Radiotherapy, Oncology and Palliative Care, Hospital Umum Sarawak (Sarawak General Hospital), Kuching Sarawak, Malaysia.
Hwoei Fen Soo HooConsultant Clinical Oncologist and Training Lead, Penang General Hospital, Pulau Pinang, Malaysia.
Tom Wei-Wu ChenGraduate Institute of Oncology, National Taiwan University College of Medicine, Taipei, Taiwan.
Suhana YusakDepartment of Radiotherapy and Oncology, National Cancer Institute, Putrajaya, Malaysia.
Rangasamy RamachandranDepartment of Clinical Oncology, University Malaya, Kuala Lumpur, Malaysia.
Najihah Abu BakarDepartment of Radiotherapy and Oncology, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia.ORCID 0009-0005-6338-4819
Ming-Huang ChenDepartment of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan.ORCID 0000-0003-3187-7393
Yasushi YatabeDepartment of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0003-1788-559X
Kenichi NakamuraDepartment of International Clinical Development, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0003-3534-8296
Hitomi Sumiyoshi OkumaDepartment of International Clinical Development, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0001-9639-7361
Kan YonemoriDepartment of International Clinical Development, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-7624-7611

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRare cancers are molecularly heterogeneous and lack robust clinical evidence to guide treatment. Whether cancer driver gene expression is governed by tumor lineage or specific somatic alterations-and whether this distinction carries clinical relevance-remains poorly characterized, particularly in Asian populations. This study aimed to determine the relative contributions of tumor lineage and DNA mutations to RNA expression of cancer driver genes and to evaluate the clinical implications of genomic alteration status in Asian patients with rare cancers.

methodsDNA and RNA were extracted from formalin-fixed paraffin-embedded tumor samples obtained through the MASTER KEY Asia research network. Next-generation sequencing was performed to evaluate genomic alterations and gene expression profiles. RNA expression of cancer driver genes was quantified as TPM

resultsIntegrated DNA and RNA data were available for 128 patients. Tumor lineage was the predominant determinant of RNA expression in 17 of 27 cancer driver genes (63%), whereas

conclusionThese findings demonstrate that genomic alteration status, including

Indexed as

MutationNeoplasmsAsian PeopleGene Expression Regulation, NeoplasticHumans

Identifiers

PMID42372207
PMCPMC13336689

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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.