Evidence map›Paper›PMID 40332491›Full record

ReviewInternational journal of molecular sciences2025

The Current Roadmap of Lung Cancer Biology, Genomics and Racial Disparity.

Enas S Alsatari, Kelly R Smith, Sapthala P Loku Galappaththi, Elba A Turbat-Herrera, Santanu Dasgupta

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
–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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Targeting KRASFrontiers in oncology · 2026
    Pooled it
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
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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

5 authors.

Enas S AlsatariDepartment of Pathology, Frederick P. Whiddon College of Medicine, University of South Alabama, Mobile, AL 36688, USA.
Kelly R SmithDepartment of Pathology, Frederick P. Whiddon College of Medicine, University of South Alabama, Mobile, AL 36688, USA.ORCID 0000-0002-6999-0845
Sapthala P Loku GalappaththiDepartment of Pathology, Frederick P. Whiddon College of Medicine, University of South Alabama, Mobile, AL 36688, USA.
Elba A Turbat-HerreraDepartment of Pathology, Frederick P. Whiddon College of Medicine, University of South Alabama, Mobile, AL 36688, USA.
Santanu DasguptaDepartment of Pathology, Frederick P. Whiddon College of Medicine, University of South Alabama, Mobile, AL 36688, USA.ORCID 0000-0002-1499-0039

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Globally, lung cancer is the most prevalent cause of cancer-related death. There are two large histological groups of lung cancer: small-cell lung cancer (SCLC) and non-small-cell lung cancer (NSCLC). Based on histopathological and molecular features, adenocarcinoma (ADC) and squamous cell carcinoma (SCC) are the two major histologic subtypes of NSCLC. Various epidemiological and environmental factors are linked with an increased risk of lung cancer. However, these risk factors show disparities in patients with divergent racial and ethnic backgrounds. Interestingly, different populations were found to harbor distinct molecular features as evidenced by variations in genetic mutation profiles. Moreover, diverse histological and molecular progression patterns are identified in lung cancer, which could be crucial in improving diagnosis, prognosis, and therapeutic planning. In concert with a plethora of nuclear genetic alterations, mitochondrial alteration, epigenetic reprogramming, microbial dysbiosis, and immune alteration signatures have been identified in various lung cancer types. This review article provides a comprehensive overview of screening tests and the treatment strategies for NSCLC and SCLC, including surgery, radiation therapy, chemotherapy, targeted therapies, and immunotherapies. Through the unification of these diverse aspects, this review article aspires to a complete understanding of lung cancer's genomics, biology, microbial landscapes, and racial disparity and seeks to understand the essential role of racial and ethnic factors in lung cancer occurrence and treatment.

Indexed as

Carcinoma, Non-Small-Cell LungGenomicsLung NeoplasmsSmall Cell Lung CarcinomaHumansgenetic mutationsimmune alterationsLUADlung cancerLUSCmitochondrial alterationsmolecular subtypesNSCLCracial disparitiesrisk factorsSCLC

Identifiers

PMID40332491
PMCPMC12027673

What Socratic 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 Socratic graph.