Somatic Landscape of Oncogenic Variants Across the Main Cancer Subtypes in Latin America: A Narrative Review.

IF 3.2 Q2 ONCOLOGY
JCO Global Oncology Pub Date : 2025-02-01 Epub Date: 2025-02-28 DOI:10.1200/GO-24-00389
Talia Wegman-Ostrosky, Lucia Taja-Chayeb, Zyanya Lucia Zatarain-Barrón, Catalina Trejo-Becerril, Daniela Shveid Gerson, Isabel Espino-Gutiérrez, Andrea Gutiérrez-Lara, Andrés Yesid Bonilla Salcedo, Mistral Castellanos Mares, José Elias García-Ortiz, Carla Daniela Robles-Espinoza, Alejandro Ruíz-Patiño
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Abstract

Variations in somatic genetic alterations can be observed across different cancer types and diverse populations. Understanding the frequency of oncogenic variants in specific populations helps elucidate carcinogenesis and risk factors, with somatic variants often serving as treatment markers. Data regarding the somatic landscape across the main tumor subtypes in patients from Latin America and the Caribbean (LAC) have increased recently, highlighting important differences from contrasting populations in North America, Europe, and Asia. Many of these differences have pressing implications regarding screening, risk factor management, targeted therapies, and health care policy. This review aims to synthesize the existing information on somatic oncogenic variants in patients' tumors from LAC. We included the frequency of somatic oncogenic variants of the most frequent tumors in LAC: prostate cancer, female breast cancer, colon cancer, gastric cancer, and lung cancer. Furthermore, we add information from tumors that are relevant in LAC because of their high incidence, specific subtypes, or aggressive phenotypes, namely gallbladder cancer, acral melanoma, and hematologic neoplasms, respectively. The data highlight distinct differences in the reported prevalences of various somatic variants across a spectrum of neoplasms. Moreover, it demonstrates that an extensive number of genetic and molecular studies have been carried out in the region, improving the level of characterization for this complex, admixed population. Nonetheless, data from many individual countries are still scarce or altogether missing, underscoring the need to establish collaborative groups to further advance progress in LAC. The need for further comprehensive research in the area should not be substituted with data from other regions as we seek to empower the choices to improve our health care outlook.

在不同癌症类型和不同人群中都能观察到体细胞基因变异。了解特定人群中致癌变异的频率有助于阐明致癌因素和风险因素,体细胞变异通常可作为治疗标记。最近,有关拉丁美洲和加勒比地区(LAC)患者主要肿瘤亚型的体细胞变异情况的数据有所增加,凸显了与北美、欧洲和亚洲不同人群的重要差异。其中许多差异对筛查、风险因素管理、靶向治疗和医疗保健政策具有迫切的影响。本综述旨在总结拉丁美洲和加勒比地区患者肿瘤中体细胞致癌变异的现有信息。我们收录了拉丁美洲和加勒比地区最常见肿瘤(前列腺癌、女性乳腺癌、结肠癌、胃癌和肺癌)中体细胞致癌变异的频率。此外,我们还添加了与拉丁美洲和加勒比地区相关的肿瘤信息,这些肿瘤因其高发病率、特定亚型或侵袭性表型而与拉丁美洲和加勒比地区相关,它们分别是胆囊癌、尖锐湿疣黑色素瘤和血液肿瘤。这些数据突显了各种体细胞变异在各种肿瘤中的报告流行率存在明显差异。此外,数据还表明,该地区已开展了大量遗传和分子研究,从而提高了对这一复杂混血人群特征的描述水平。然而,许多国家的数据仍然稀缺或完全缺失,这突出表明有必要建立合作小组,以进一步推动拉丁美洲和加勒比地区的研究进展。我们需要在这一领域开展进一步的综合研究,但我们不应以其他地区的数据来取代我们的研究,因为我们需要做出选择,以改善我们的医疗保健前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JCO Global Oncology
JCO Global Oncology Medicine-Oncology
CiteScore
6.70
自引率
6.70%
发文量
310
审稿时长
7 weeks
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