Evidence map›Paper›PMID 37719881›Full record

ArticleFrontiers in cell and developmental biology2023

Molecular typing and prognostic risk models for ovarian cancer: a study based on cell differentiation trajectory.

Tingfeng Chen, Tingting Ni, Lan Mu, Zhou Ying, Hanqun Zhang, Zi Wang

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In one paragraph

Article in Frontiers in cell and developmental biology, 2023. 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Tingfeng Chen *Department of Oncology, Guizhou Provincial People's Hospital, Guiyang, China.
Tingting Ni *Department of Oncology, Guizhou Provincial People's Hospital, Guiyang, China.
Lan MuDepartment of Oncology, Guizhou Provincial People's Hospital, Guiyang, China.
Zhou YingDepartment of Medical Records and Statistics, Guizhou Provincial People's Hospital, Guiyang, China.
Hanqun ZhangDepartment of Oncology, Guizhou Provincial People's Hospital, Guiyang, China.
Zi WangDepartment of Oncology, Guizhou Provincial People's Hospital, Guiyang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer is a heterogeneous disease with different molecular phenotypes. We performed molecular typing of ovarian cancer using cell differentiation trajectory analysis and proposed a prognostic risk scoring model. Using the copy number variation provided by inferCNV, we identified malignant tumor cells. Then, ovarian cancer samples were divided into four subtypes based on differentiation-related genes (DRGs). There were significant differences in survival rates, clinical features, tumor microenvironment scores, and the expression levels of ICGs among the subtypes. Based on nine DRGs, a prognostic risk score model was generated (AUC at 1 year: 0.749; 3 years: 0.651). Then we obtained a nomogram of the prognostic variable combination, including risk scores and clinicopathological characteristics, and predicted the 1-, 3- and 5-year overall survival. Finally, we explored some issues of immune escape using the established risk model. Our study demonstrates the significant influence of cell differentiation on predicting prognosis in OV patients and provides new insights for OV treatment and potential immunotherapeutic strategies.

Indexed as

bioinformaticscell differentiation trajectorymolecular typingovarian cancersingle cell

Identifiers

PMID37719881
PMCPMC10500593

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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.