Evidence map›Paper›PMID 40427695›Full record

ReviewBiology2025

Radon Exposure and Cancer Risk: Assessing Genetic and Protein Markers in Affected Populations.

Yerlan Kashkinbayev, Baglan Kazhiyakhmetova, Nursulu Altaeva, Meirat Bakhtin, Pavel Tarlykov, Elena Saifulina, Moldir Aumalikova, Danara Ibrayeva, Aidos Bolatov

Abstract readReview
In one paragraph

Review in Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. 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.

Yerlan KashkinbayevInstitute of Radiobiology and Radiation Protection, Astana Medical University, Astana 010000, Kazakhstan.ORCID 0000-0002-6095-459X
Baglan KazhiyakhmetovaInstitute of Radiobiology and Radiation Protection, Astana Medical University, Astana 010000, Kazakhstan.
Nursulu AltaevaMedical Genetics and Molecular Biology Department, Astana Medical University, Astana 010000, Kazakhstan.
Meirat BakhtinInstitute of Radiobiology and Radiation Protection, Astana Medical University, Astana 010000, Kazakhstan.
Pavel TarlykovNational Center for the Biotechnology, Astana 010000, Kazakhstan.ORCID 0000-0003-2075-307X
Elena SaifulinaInstitute of Radiobiology and Radiation Protection, Astana Medical University, Astana 010000, Kazakhstan.ORCID 0000-0002-1791-0137
Moldir AumalikovaInstitute of Radiobiology and Radiation Protection, Astana Medical University, Astana 010000, Kazakhstan.
Danara IbrayevaInstitute of Radiobiology and Radiation Protection, Astana Medical University, Astana 010000, Kazakhstan.ORCID 0000-0002-1640-1728
Aidos BolatovSchool of Medicine, Shenzhen University, Shenzhen 518060, China.ORCID 0000-0002-5390-4623

Funding

Committee of Science of the Ministry of Science and Higher Education of the Republic of Kazakhstan IRN AP22786933ERAN x-25-xx.
6 · The paper itself

Abstract

Radon is an inert gas produced by the radioactive decay of uranium-238, commonly found in the environment. Radon and its decay products are the main sources of human exposure to radiation from natural sources. When inhaled, radon's alpha particles impact lung tissue, potentially causing lung cancer by damaging DNA and altering oxidative processes. This review article addresses the need for a deeper understanding of the genetic and molecular changes associated with radon-induced lung cancer, aiming to clarify key genetic mutations and protein markers linked to carcinogenesis. Particular attention in recent studies has been given to mutations in tumor suppressor genes (RASSF1, TP53), oncogenes (KRAS, EGFR), and changes in the expression levels of protein biomarkers associated with inflammation, stress, and apoptosis. Identifying these markers is critical for developing effective screening methods for radon-induced lung cancer, enabling timely identification of high-risk patients and supporting effective preventive strategies. Summarizing current genetic and protein biomarkers, this review highlights the importance of a comprehensive approach to studying radon-induced carcinogenesis. Understanding these molecular mechanisms could ultimately improve early diagnostic methods and enhance therapy for cancers associated with radon exposure.

Indexed as

epigenetic changesgeneslung cancerprotein markersradon

Identifiers

PMID40427695
PMCPMC12109156

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.