Evidence map›Paper›PMID 36175592›Full record

ArticleMedical oncology (Northwood, London, England)2022

Association between cancer genes and germ layer specificity.

Hwayeong Lee, Sungwhan Lee, Woo Jong Cho, Minjung Shin, Leeyoung Park

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 1 country.

Hwayeong Lee *Natural Science Research Institute, Yonsei University, 134 Shinchon-Dong, Seodaemun-Ku, Seoul, 120-749, Korea.
Sungwhan Lee *Natural Science Research Institute, Yonsei University, 134 Shinchon-Dong, Seodaemun-Ku, Seoul, 120-749, Korea.
Woo Jong ChoNatural Science Research Institute, Yonsei University, 134 Shinchon-Dong, Seodaemun-Ku, Seoul, 120-749, Korea.
Minjung ShinNatural Science Research Institute, Yonsei University, 134 Shinchon-Dong, Seodaemun-Ku, Seoul, 120-749, Korea.
Leeyoung ParkNatural Science Research Institute, Yonsei University, 134 Shinchon-Dong, Seodaemun-Ku, Seoul, 120-749, Korea. lypark@yonsei.ac.kr.ORCID http://orcid.org/0000-0003-3691-822X
Yonsei University · KREwha Womans University · KR

Funding

Korea Institute of Science and Technology Information KSC-2017-C3-0052the National Research Foundation of Korea 2015K1A3A1A14021223the National Research Foundation of Korea 2018K1A3A7A08089881the National Research Foundation of Korea 2018R1D1A1B07042910
6 · The paper itself

Abstract

Cancer signaling pathways defining cell fates are related to differentiation. During the developmental process, three germ layers (endoderm, mesoderm, and ectoderm) are formed during embryonic development that differentiate into organs via the epigenetic regulation of specific genes. To examine the relationship, the specificities of cancer gene mutations that depend on the germ layers are studied. The major organs affected by cancer were determined based on statistics from the National Cancer Information Center of Korea, and were grouped according to their germ layer origins. Then, the gene mutation frequencies were evaluated to identify any bias based on the differentiation group using the Catalogue of Somatic Mutations in Cancer (COSMIC) database. The chi-square test showed that the p-value of 152 of 166 genes was less than 0.05, and 151 genes showed p-values of less than 0.05 even after adjusting for the false discovery rate (FDR). The germ layer-specific genes were evaluated using visualization based on basic statistics, and the results matched the top ranking genes depending on organs in the COSMIC database.The current study confirmed the germ layer specificity of major cancer genes. The germ layer specificity of mutated driver genes is possibly important in cancer treatments because each mutated gene may react differently depending on the germ layer of origin. By understanding the mechanism of gene mutation in the development and progression of cancer in the context of cell-fate pathways, a more effective therapeutic strategy for cancer can be established.

Indexed as

Epigenesis, GeneticNeoplasmsDatabases, FactualFemaleGenes, NeoplasmGerm LayersHumansMutationPregnancyCancer geneCancer organCell-fate pathwayCOSMIC databaseGerm layer

Identifiers

PMID36175592
OpenAlexW4297989879

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.