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结直肠癌中的遗传和表观遗传肿瘤内异质性

Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer.

作者信息

Jones Huw Geraint, Jenkins Gareth, Williams Namor, Griffiths Paul, Chambers Phil, Beynon John, Harris Dean

机构信息

Department of Colorectal Surgery, Singleton Hospital, Abertawe Bro Morgannwg University Local Health Board, Sketty Lane, Swansea, SA2 8QA, UK.

, 16 Forrest Road, Canton, Cardiff, CF5 1HR, UK.

出版信息

World J Surg. 2017 May;41(5):1375-1383. doi: 10.1007/s00268-016-3860-z.

Abstract

INTRODUCTION

Colorectal cancer (CRC) is a highly heterogeneous disease, with pathologically similar cancers having completely different responses to treatment and patient survival. Intra-tumour heterogeneity (defined as distinct morphological and phenotypic differences) has recently been demonstrated to be an important factor in the development and behaviour of cancer cells and can be used to determine response to anticancer therapy.

METHOD

Patients with resected CRC had DNA extracted from eight defined tumour areas which were analysed for two genetic mutations (BRAF and KRAS) and one epigenetic trait (CpG island methylator phenotype/CIMP). Normal adjacent tissue was studied as control.

RESULTS

Twelve patients with CRC were included. Intra-tumoural heterogeneity for KRAS mutation was seen in 2 patients (17%). There was no statistical evidence of CIMP status heterogeneity (p = 0.85), but 6 of the 12 patients (50%) demonstrated at least one heterogeneous area within the tumour.

DISCUSSION

Intra-tumoural heterogeneity for both genetic and epigenetic factors in CRC is more prevalent than previously thought in Stage II and Stage III CRC. This study provides new insight into epigenetic heterogeneity of CRC and supports the development of a more targeted biopsy strategy to support expansion of personalised treatment.

摘要

引言

结直肠癌(CRC)是一种高度异质性疾病,病理上相似的癌症对治疗的反应和患者生存率却完全不同。肿瘤内异质性(定义为明显的形态学和表型差异)最近已被证明是癌细胞发生和行为的一个重要因素,可用于确定对抗癌治疗的反应。

方法

对接受手术切除的CRC患者,从八个明确的肿瘤区域提取DNA,分析两种基因突变(BRAF和KRAS)和一种表观遗传特征(CpG岛甲基化表型/CIMP)。以相邻正常组织作为对照进行研究。

结果

纳入12例CRC患者。2例患者(17%)出现KRAS突变的肿瘤内异质性。没有统计学证据表明CIMP状态存在异质性(p = 0.85),但12例患者中有6例(50%)在肿瘤内至少有一个异质区域。

讨论

在II期和III期CRC中,CRC的遗传和表观遗传因素的肿瘤内异质性比以前认为的更为普遍。本研究为CRC的表观遗传异质性提供了新的见解,并支持制定更具针对性的活检策略,以推动个性化治疗的扩展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22f0/5394146/0ee88db4ee8f/268_2016_3860_Fig1_HTML.jpg

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