Evidence map›Paper›PMID 38316717›Full record

ArticleGenes & genomics2024

Genetic specificity study using next-generation sequencing (NGS) of peritoneal metastatic colorectal cancer compared to primary colorectal cancer.

Sungchul Lee, Wonseok Shin, Dong-Guk Park, Hwan Namgung

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Article in Genes & genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2 citing papers in PubMed.

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5 · Who and what money

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4 authors.

Sungchul Lee *Department of Surgery, Dankook University College of Medicine, Cheonan, Republic of Korea.
Wonseok Shin *NGS Clinical Laboratory, Division of Cancer Research, Dankook University Hospital, Cheonan, Republic of Korea.
Dong-Guk ParkDepartment of Surgery, Dankook University College of Medicine, Cheonan, Republic of Korea.
Hwan NamgungDepartment of Surgery, Dankook University College of Medicine, Cheonan, Republic of Korea. gsnamgung@dankook.ac.kr.

Funding

Ministry of Education NRF-RS-2023-00275307
6 · The paper itself

Abstract

backgroundIn patients with colorectal cancer, peritoneal metastases are the second most frequent metastatic lesion after liver metastases. Peritoneal metastases have a very poor prognosis, with a median survival time of 5-7 months. Currently, there is a lack of research on the genetic differences between primary colorectal cancer and peritoneal metastases. Therefore, we aimed to identify their genetic characteristics through a cancer panel test using next-generation sequencing.

objectiveWe aim to investigate the specificity of genetic variants in primary colorectal cancer and peritoneal metastases.

methodsWe recruited patients with stage I, II, and III primary colorectal cancer and peritoneal metastases for genetic analysis using NGS. Samples were collected from patients who underwent surgery at Dankook University Hospital and consented to genetic testing. NGS was performed using a cancer panel.

resultsAmong 36 patients with primary cancer, TP53 gene mutation was identified the most in 25 patients (69%), followed by APC gene mutation in 19 patients (53%), and KRAS gene mutation in 17 patients (47%). In the peritoneal metastasis patient group, unlike the primary cancer patient group, KRAS gene mutations were the most common 6 patients (55%), followed by TP53 gene mutations in 4 patients (36%) and PIK3CA gene mutations in 2 patients (18%).

conclusionThe small number of surgical cases of peritoneal metastases was a limitation of our sample size. Nevertheless, we identified differences in the alterations of specific genes between primary and peritoneal metastases. Acquiring additional cases and collecting more data will provide deeper insights into these cancers.

Indexed as

Colonic NeoplasmsColorectal NeoplasmsPeritoneal NeoplasmsRectal NeoplasmsHigh-Throughput Nucleotide SequencingHumansMutationProto-Oncogene Proteins p21(ras)Proto-Oncogene Proteins p21(ras)Colorectal cancerGene mutationNext-generation sequencingPeritoneal metastasis

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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.