Lynch syndrome-associated endometrial cancer: prevention, screening and prognosis
Lynch syndrome-associated endometrial cancer: prevention, screening and prognosis
批准号:
MR/M018431/1
负责人:
Neil Andrew Ryan
金额:
$27.67万
依托单位:
依托单位国家:
英国
项目类别:
Fellowship
财政年份:
2015
资助国家:
英国
项目状态:
已结题
起止时间:
2015 至 --
中文摘要
林奇综合征是由特定的基因缺陷引起的,这些基因缺陷使癌症更容易发生。林奇综合症有家族遗传。肠癌和子宫癌在林奇综合征患者中更常见。当我们知道有人患有林奇综合征时,我们提供结肠镜检查,一种观察肠道内部的相机测试,以在癌变之前切除任何肠息肉。这已被证明可以挽救生命。为了预防子宫癌,一些女性在家庭完整后会进行子宫切除术。其他人有子宫癌筛查或采取激素治疗,即使我们不知道这些东西是否有效。多达十分之一的子宫癌患者可能患有Lynch综合征,尽管大多数人并不知道。如果他们知道Lynch综合征,他们可能会选择通过结肠镜定期筛查以切除肠息肉。他们还可以帮助其他家庭成员发现他们是否患有林奇综合征。患有Lynch综合征的女性中发生的子宫癌可能表现不同,并且与没有Lynch综合征的女性中发生的子宫癌相比具有不同的前景。在这个项目中,我将进行三项研究:在研究1中,我将观察有多少子宫癌患者患有他们不知道的林奇综合征。我们可以通过对肿瘤进行特定的实验室测试来发现这一点。我将观察200名妇女,她们在接受子宫切除术时为未来的研究项目提供了血液和肿瘤样本。我还将对200名新诊断为子宫癌的妇女进行测试,因为她们正在接受手术。如果肿瘤研究表明可能存在林奇综合征,我们将进行血液检查,看看是否存在基因故障。这将在储存的血液样本上进行,或者对于目前的患者,将通过我们医院的遗传咨询服务进行基因检测。我们将发现有多少患有子宫癌的女性患有林奇综合征。我还将发现测试患有子宫癌的女性是否患有林奇综合征是多么简单。我将看看患者是否愿意接受林奇综合征的肿瘤检测,以及他们是否准备接受遗传咨询。我会看看他们是否愿意接受结肠镜检查,以确定和治疗肠息肉。我也会看到多少筛查林奇综合征的妇女与子宫癌可能会花费。这将有助于我们制定未来子宫癌患者应进行林奇综合征测试的指南。 在研究2中,我将比较患有林奇综合征的妇女和没有患林奇综合征的妇女的子宫癌。使用专业的实验室技术,我将看看肿瘤是如何不同的,以及它们是如何相同的。我将研究患有林奇综合征的妇女是否比没有林奇综合征的妇女更容易或更不容易死于子宫癌。这将有助于我们更多地了解子宫癌,并在未来更好地告知患者。 研究3将研究子宫癌筛查和激素治疗在预防Lynch综合征妇女子宫癌方面的有效性。我将看看超重和不活动是否会使患林奇综合征的妇女更容易患子宫癌。这将有助于我们在女性知道自己患有林奇综合征时给予适当的建议。
英文摘要
Lynch syndrome is caused by specific gene faults that make cancer more likely to occur. Lynch syndrome runs in families. Bowel cancer and womb cancer are more common in people with Lynch syndrome. When we know someone has Lynch syndrome, we offer colonoscopy, a camera test to look inside the bowel, to remove any bowel polyps before they become cancerous. This has been shown to save lives. To prevent womb cancer, some women have a hysterectomy once their family is complete. Others have womb cancer screening or take hormone treatments, even though we do not know if these things work. As many as 1 in 10 women with womb cancer may have Lynch syndrome, although most do not know it. If they knew about the Lynch syndrome, they may choose to have regular screening by colonoscopy to remove bowel polyps. They may also help other family members find out whether they have Lynch syndrome. Womb cancer that develops in women with Lynch syndrome may behave differently and have a different outlook compared with womb cancer that occurs in women without Lynch syndrome. No one has looked at this before.In this project, I will be conducting three studies: In Study 1, I will see how many patients with womb cancer have Lynch syndrome that they didn't know about. We can find this out by carrying out specific laboratory tests on the tumours. I will look at 200 women who gave blood and tumour samples for future research projects when they came in for their hysterectomy. I will also test 200 women with new diagnoses of womb cancer as they come through the department for their surgery. If the tumour studies suggest that Lynch syndrome may be present, we will carry out blood tests to see if the gene fault is there. This will be done on the stored blood sample or, for current patients, genetic testing will be carried out through the genetic counselling service in our hospital. We will find out how many women with womb cancer have Lynch syndrome. I will also find out how straightforward it is to test women with womb cancer for Lynch syndrome. I will see whether patients are happy for their tumours to be tested for Lynch syndrome and whether they are prepared to go for genetic counselling. I will see whether they want to undergo colonoscopy to identify and treat bowel polyps. I will also see how much screening for Lynch syndrome in women with womb cancer is likely to cost. This will help us develop guidelines for which patients with womb cancer should be tested for Lynch syndrome in the future. In Study 2, I will compare womb cancers from women who have Lynch syndrome with those who do not. Using specialised laboratory techniques, I will look to see how the tumours are different and how they are the same. I will look at whether the women with Lynch syndrome were more or less likely to die from their womb cancer than women without. This will help us understand womb cancer more and inform patients better in the future. Study 3 will look at how effective womb cancer screening and hormone treatments are at preventing womb cancer in women with Lynch syndrome. I will see whether being overweight and inactive make womb cancer more likely in women with Lynch syndrome. This will help us advise women properly when they know they have Lynch syndrome.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1158/1940-6207.capr-21-0229
发表时间:
2021-11
期刊:
Cancer prevention research (Philadelphia, Pa.)
影响因子:
--
作者:
[]
通讯作者:
DOI:
10.3390/cancers13215444
发表时间:
2021-10-29
期刊:
Cancers
影响因子:
5.2
作者:
[Barr CE, Njoku K, Hotchkies L, Ryan NAJ, Wan YL, Davies DA, Razvi S, Crosbie EJ]
通讯作者:
Crosbie EJ
DOI:
10.1136/jmedgenet-2020-107270
发表时间:
2021-10
期刊:
Journal of medical genetics
影响因子:
4
作者:
[Crosbie EJ, Ryan NAJ, McVey RJ, Lalloo F, Bowers N, Green K, Woodward ER, Clancy T, Bolton J, Wallace AJ, McMahon RF, Evans DG]
通讯作者:
Evans DG
国内基金
海外基金
登录
查看更多内容
骨髓ISG+NAMPT+中性粒细胞介导抗磷脂综合征B细胞异常活化的机制研究
-
批准号:82371799
-
项目类别:面上项目
-
资助金额:47.00万元
-
批准年份:2023
-
负责人:杨程德
-
依托单位:
胆固醇合成蛋白CYP51介导线粒体通透性转换诱发Th17/Treg细胞稳态失衡在舍格伦综合征中的作用机制研究
-
批准号:82370976
-
项目类别:面上项目
-
资助金额:48.00万元
-
批准年份:2023
-
负责人:郑凌艳
-
依托单位:
多囊卵巢综合征中甲酰肽受体2调控小胶质细胞代谢重编程导致GnRH神经元过度激活及HPO轴异常的病理机制研究
-
批准号:82370797
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:陶弢
-
依托单位:
肥大细胞与脂肪细胞互作调控长期高脂饮食小鼠附睾脂肪组织萎缩重构的机制
-
批准号:32070757
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:刘健
-
依托单位:
去唾液酸糖蛋白受体1(ASGR1)调控脂质转运的分子机制及其在非酒精性脂肪肝炎中的作用研究
-
批准号:31900539
-
项目类别:青年科学基金项目
-
资助金额:20.0万元
-
批准年份:2019
-
负责人:徐莹莹
-
依托单位:
ISLR参与肥胖小鼠胰岛素抵抗的机制研究
-
批准号:31970712
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2019
-
负责人:孟庆勇
-
依托单位:
利用带内源标签的小鼠研究SREBP通路调控肝癌发生发展的分子机制
-
批准号:31900541
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2019
-
负责人:李钠
-
依托单位:
谷氨酰胺酶抑制剂与敲除lncRNA NCRNA00219联合抗肿瘤的研究
-
批准号:31900540
-
项目类别:青年科学基金项目
-
资助金额:15.0万元
-
批准年份:2019
-
负责人:廖梅坚
-
依托单位:
卡路里限制的T细胞糖脂代谢重塑机制及网络调控
-
批准号:91957111
-
项目类别:重大研究计划
-
资助金额:80.0万元
-
批准年份:2019
-
负责人:李佩盈
-
依托单位:
Perry syndrome相关蛋白p150glued调控黑质多巴胺能神经元功能和变性的机制
-
批准号:81601117
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:于佳
-
依托单位: