Evidence map›Paper›PMID 41465076›Full record

ReviewGenes2025

Addressing Ancestral Underrepresentation in Oncobiology: The Need for Sub-Saharan African-Specific In Vitro Models.

Carla S Dos Santos, Ana C Magalhães, Ricardo J Pinto, Carla Carrilho, Cláudia Pereira, Fernando Miguel, Pamela Borges, Lúcio Lara Santos, Luisa Pereira

Abstract readReview
In one paragraph

Review in Genes, 2025. 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

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

9 authors.

Carla S Dos Santosi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-0960-4818
Ana C Magalhãesi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
Ricardo J Pintoi3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
Carla CarrilhoDepartment of Pathology, Faculty of Medicine, Eduardo Mondlane University, Maputo 2HJP+QWV, Mozambique.ORCID 0000-0003-0208-7309
Cláudia PereiraUnidade Local de Saúde Almada-Seixal, 2805-267 Almada, Portugal.
Fernando MiguelAngolan Institute Against Cancer, Luanda 56FG+7R6, Angola.
Pamela BorgesMolecular Biology Laboratory, Hospital Universitário Agostinho Neto, Praia 112, Cape Verde.ORCID 0000-0002-4491-9874
Lúcio Lara SantosGrupo de Patologia e Terapêutica Experimental e Departamento de Oncologia do Instituto Português de Oncologia do Porto, 4200-072 Porto, Portugal.ORCID 0000-0002-0521-5655
Luisa Pereirai3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-4271-1527

Funding

FCT-Fundação para a Ciência e a Tecnologia SFRH/BD/145217/2019FEDER-Fundo Europeu de Desenvolvimento Regional PTDC/BIA-MOL/3986/2021Liga Portuguesa Contra o Cancro-Núcleo Regional do Norte Bolsas LPCC-NRN 2024
6 · The paper itself

Abstract

Cancer is an increasing public health burden, including in Sub-Saharan African (SSA) populations, where cancer incidence is predicted to increase by around 140% between 2022 and 2050. These rates require a better understanding of the epidemiological, clinical, and genetic/molecular characteristics of cancer in SSA populations. There is an urgent need to improve the genomic characterization of SSA tumour samples and also to establish suitable in vitro models for hypothesis testing. In fact, even though thousands of cancer cell lines (CCLs) have been established employing different methods of cell immortalization and have been included in deep molecular characterization panels, SSA ancestry is limited to only ~6% (mostly African Americans, who represent limited diversity in the context of the African continent) of publicly available CCLs. This disparity needs to be addressed by using next-generation immortalization methods such as conditional reprogramming to establish CCLs derived from SSA cancer patients that also represent the diversity within the African continent. Research in SSA oncobiology has the potential to add essential information to better understand the diverse molecular pathways leading to cancer and to find promising therapeutic avenues. We also discuss the challenges to conducting oncobiology studies with cell modelling derived from SSA patients in low-to-middle-income African countries, such as Portuguese-speaking African countries.

Indexed as

NeoplasmsAfrica South of the SaharaBlack or African AmericanBlack PeopleCell Line, TumorHumanscancer cell linesconditional reprogrammingin vitro modelsoncology researchSub-Saharan Africa

Identifiers

PMID41465076
PMCPMC12732366

What OpenQuestion 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 OpenQuestion graph.