Evidence map›Paper›PMID 41364205›Full record

ReviewArchives of microbiology2025

Molecular links between tuberculosis and lung cancer: pathogenesis and therapeutic challenges.

Francis Adu-Amankwaah, Suzzana Dickson Buabeng, Isabella Sanette Agyekum, Ndivhuwo Tshililo, Lucinda Baatjies, Bienyameen Baker

Abstract readReview
PubMed Publisher
In one paragraph

Review in Archives of microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Francis Adu-Amankwaah *DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa. fa@sun.ac.za.
Suzzana Dickson Buabeng *DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa. bbnsuz001@myuct.ac.za.
Isabella Sanette AgyekumDepartment of Global Health, African Cancer Institute, Stellenbosch University, Cape Town, South Africa.
Ndivhuwo TshililoDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Lucinda BaatjiesDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Bienyameen BakerDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research, South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa. brubaker@sun.ac.za.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis (TB) and lung cancer, two leading global health burdens, increasingly coexist, particularly in high-burden regions of these diseases. Epidemiological studies suggest TB significantly elevates lung cancer risk, as lung cancer increases the risk of TB, yet the molecular basis of this association remains underexplored. TB-induced chronic inflammation, oxidative stress, epithelial-mesenchymal transition (EMT), and immune checkpoint dysregulation create a permissive environment for oncogenesis. Granulomas and tumour microenvironments share immunosuppressive features, while overlapping host genetic and epigenetic signatures exacerbate diagnostic complexity. Immunotherapy in cancer risks TB reactivation, highlighting clinical tensions. Understanding the TB-lung cancer molecular interface is essential for developing integrated diagnostics and safe treatment regimens. This review integrates current evidence on the overlapping pathogenic, immunological and molecular landscapes of TB and lung cancer to identify shared mechanisms, diagnostic dilemmas and therapeutic challenges, while highlighting significant gaps needing actionable interventions. We also suggest some future paradigm shifts toward dual-disease research frameworks, critical to advance care in TB-endemic regions.

Indexed as

Lung NeoplasmsTuberculosisAnimalsEpithelial-Mesenchymal TransitionHumansMycobacterium tuberculosisTumor MicroenvironmentBiomarker discoveryHost-directed therapyInflammationLung cancerMolecular pathwayTuberculosis (TB)

Identifiers

What OpenQuestion holds

Textmetadata
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.