Lingyi Yang, Lin Gao, Ruiqi Qian, Xiuqin Zhang, Xurui Shen
{"title":"肺腺癌患者肝转移的特异性基因组改变和分子机制。","authors":"Lingyi Yang, Lin Gao, Ruiqi Qian, Xiuqin Zhang, Xurui Shen","doi":"10.1080/07357907.2025.2558087","DOIUrl":null,"url":null,"abstract":"<p><p>Given the limited diagnostic technologies and treatment options available for lung adenocarcinoma (LUAD) patients with liver metastases, it is crucial to identify potential genomic signatures associated with liver metastasis, which could significantly contribute to the development of improved diagnostic tools and treatment strategies for LUAD patients with liver metastases. In this study, we identified specific genetic alterations in tumor samples with liver metastases by targeted capture sequencing. The results showed that the significantly higher mutation frequencies of <i>KRAS</i>, <i>STK11</i> and <i>ERBB2</i> in LUAD patients with liver metastases and <i>ERBB2</i> and <i>STK11</i> mutations found in both tumor tissues and plasma samples from patients with liver metastases. In addition, the higher mutation frequencies of <i>KRAS</i> and <i>STK11</i> in the group with early-stage liver metastasis suggested that mutations in <i>KRAS</i> and <i>STK11</i> may play crucial roles in promoting liver metastases in LUAD patients at an early stage. Furthermore, the significantly higher TMB in the late-stage liver metastasis group indicated that patients with late-stage liver metastasis may have a better response to immunotherapy compared to those with early-stage liver metastasis. These findings provide valuable insights for developing detection tools and tailoring individualized treatments for such patients.</p>","PeriodicalId":9463,"journal":{"name":"Cancer Investigation","volume":" ","pages":"1-13"},"PeriodicalIF":1.9000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Specific Genomic Alterations and Molecular Mechanisms of Liver Metastases in Patients with Lung Adenocarcinoma.\",\"authors\":\"Lingyi Yang, Lin Gao, Ruiqi Qian, Xiuqin Zhang, Xurui Shen\",\"doi\":\"10.1080/07357907.2025.2558087\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Given the limited diagnostic technologies and treatment options available for lung adenocarcinoma (LUAD) patients with liver metastases, it is crucial to identify potential genomic signatures associated with liver metastasis, which could significantly contribute to the development of improved diagnostic tools and treatment strategies for LUAD patients with liver metastases. In this study, we identified specific genetic alterations in tumor samples with liver metastases by targeted capture sequencing. The results showed that the significantly higher mutation frequencies of <i>KRAS</i>, <i>STK11</i> and <i>ERBB2</i> in LUAD patients with liver metastases and <i>ERBB2</i> and <i>STK11</i> mutations found in both tumor tissues and plasma samples from patients with liver metastases. In addition, the higher mutation frequencies of <i>KRAS</i> and <i>STK11</i> in the group with early-stage liver metastasis suggested that mutations in <i>KRAS</i> and <i>STK11</i> may play crucial roles in promoting liver metastases in LUAD patients at an early stage. Furthermore, the significantly higher TMB in the late-stage liver metastasis group indicated that patients with late-stage liver metastasis may have a better response to immunotherapy compared to those with early-stage liver metastasis. These findings provide valuable insights for developing detection tools and tailoring individualized treatments for such patients.</p>\",\"PeriodicalId\":9463,\"journal\":{\"name\":\"Cancer Investigation\",\"volume\":\" \",\"pages\":\"1-13\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer Investigation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/07357907.2025.2558087\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Investigation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/07357907.2025.2558087","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
The Specific Genomic Alterations and Molecular Mechanisms of Liver Metastases in Patients with Lung Adenocarcinoma.
Given the limited diagnostic technologies and treatment options available for lung adenocarcinoma (LUAD) patients with liver metastases, it is crucial to identify potential genomic signatures associated with liver metastasis, which could significantly contribute to the development of improved diagnostic tools and treatment strategies for LUAD patients with liver metastases. In this study, we identified specific genetic alterations in tumor samples with liver metastases by targeted capture sequencing. The results showed that the significantly higher mutation frequencies of KRAS, STK11 and ERBB2 in LUAD patients with liver metastases and ERBB2 and STK11 mutations found in both tumor tissues and plasma samples from patients with liver metastases. In addition, the higher mutation frequencies of KRAS and STK11 in the group with early-stage liver metastasis suggested that mutations in KRAS and STK11 may play crucial roles in promoting liver metastases in LUAD patients at an early stage. Furthermore, the significantly higher TMB in the late-stage liver metastasis group indicated that patients with late-stage liver metastasis may have a better response to immunotherapy compared to those with early-stage liver metastasis. These findings provide valuable insights for developing detection tools and tailoring individualized treatments for such patients.
期刊介绍:
Cancer Investigation is one of the most highly regarded and recognized journals in the field of basic and clinical oncology. It is designed to give physicians a comprehensive resource on the current state of progress in the cancer field as well as a broad background of reliable information necessary for effective decision making. In addition to presenting original papers of fundamental significance, it also publishes reviews, essays, specialized presentations of controversies, considerations of new technologies and their applications to specific laboratory problems, discussions of public issues, miniseries on major topics, new and experimental drugs and therapies, and an innovative letters to the editor section. One of the unique features of the journal is its departmentalized editorial sections reporting on more than 30 subject categories covering the broad spectrum of specialized areas that together comprise the field of oncology. Edited by leading physicians and research scientists, these sections make Cancer Investigation the prime resource for clinicians seeking to make sense of the sometimes-overwhelming amount of information available throughout the field. In addition to its peer-reviewed clinical research, the journal also features translational studies that bridge the gap between the laboratory and the clinic.