Evidence map›Paper›PMID 30821106›Full record

ArticleCancer medicine2019

Comprehensive analysis of age-related somatic mutation profiles in Chinese young lung adenocarcinoma patients.

Bo Yang, Jie Li, Fang Li, Hongxia Zhou, Weiwei Shi, Huaiyin Shi, Shengjie Sun, Wending Sun, Jinliang Wang, Junxun Ma and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

19 citing papers in PubMed, 23 citations in OpenAlex.

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  15. [Current Situation of Clinical Feature and Gene Phenotype of Young Adult Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2020
    Review
  16. Article
  17. Article
  18. Review
  19. Value of serum tumor markers in early differential diagnosis of spinal tumors and spinal infections.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
    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

13 authors at 2 institutions in 1 country.

Bo YangDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.
Jie LiDepartment of Pathology, General Hospital of Chinese PLA, Beijing, China.
Fang LiDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.
Hongxia ZhouGenomiCare Biotechnology Co. Ltd., Shanghai, China.
Weiwei ShiDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.
Huaiyin ShiDepartment of Pathology, General Hospital of Chinese PLA, Beijing, China.
Shengjie SunDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.
Wending SunGenomiCare Biotechnology Co. Ltd., Shanghai, China.
Jinliang WangDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.
Junxun MaDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.
Xiang YanDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.
Yi HuDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.
Shunchang JiaoDepartment of Oncology, General Hospital of Chinese PLA, Beijing, China.ORCID 0000-0001-5049-5492
Chinese PLA General Hospital · CNGenomiCare (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung adenocarcinoma in young adults is a rare entity with the oncogenic genetic alterations associated being poorly understood. In the present study, the effect of genetic alterations in lung adenocarcinoma patients diagnosed in young patients is reported.

methodsTwenty young lung adenocarcinoma patients (age years: median: 33.5, range: 24-36) were enrolled in the current study and 24 patients who were at common age of the disease onset (age years: median: 61.5, range: 52-79) were selected for comparison. Paraffin sections of lung adenocarcinoma were analyzed using the whole-exome sequencing platform.

resultsSimilar number of somatic mutations per tumor were found in the young patients and their older counterparts. Although no age-related differences were detected in the numbers of lung adenocarcinoma patients harboring well-known gene variants, mutations in FRG1 and KMT2C were associated with a younger age especially after correcting for tobacco smoking and sex (FRG1: P = 0.027, KMT2C: P = 0.046). Five genetic variants showed higher alteration frequencies in young patients compared to the unclassified East Asian population, suggesting these mutations as disease-related hereditary germline variants.

conclusionsThese results suggest different characteristics of lung adenocarcinoma between the young and the patients at common age of onset. Young patients with lung adenocarcinoma have a distinctly unique prevalence of oncogenic genetic alterations.

Indexed as

MutationAdenocarcinoma of LungAdultAgedAsian PeopleDNA-Binding ProteinsExome SequencingFemaleHigh-Throughput Nucleotide SequencingHumansLung NeoplasmsMaleMicrofilament ProteinsMiddle AgedRNA-Binding ProteinsSex FactorsDNA-Binding ProteinsFRG1 protein, humanKMT2C protein, humanMicrofilament ProteinsRNA-Binding Proteinsage-related dimorphismlung adenocarcinomaoncogenic genetic alterationswhole-exome sequencingyounger adults

Identifiers

PMID30821106
PMCPMC6488136
OpenAlexW2919606018

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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.