High expression of L-type amino acid transporter 1 (LAT1) predicts poor prognosis in pancreatic ductal adenocarcinomas

High expression of L-type amino acid transporter 1 (LAT1) predicts poor prognosis in pancreatic ductal adenocarcinomas
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DOI:
10.1136/jclinpath-2012-200826
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发表时间:
2012-11-01
影响因子:
3.4
通讯作者:
Okayasu, Isao
Okayasu, Isao
中科院分区:
医学3区
文献类型:
--
作者:
Yanagisawa, Nobuyuki;Ichinoe, Masaaki;Okayasu, Isao

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背景与目的针对L型氨基酸转运蛋白1(LAT 1)的分子靶向治疗是目前唯一的靶向治疗方法,具有广阔的发展前景。LAT 1表达在胰腺癌中作为预后预测因子进行了研究。方法采用免疫组化方法对66例手术切除的胰腺导管腺癌(PDAC,n = 66)进行研究。作为参考,导管内乳头状粘液癌(IPMC,包括导管内乳头状粘液瘤(IPMN)与高度异型增生或与相关的浸润性癌,n = 13)和腺瘤(IPMA,包括IPMN与低,中级异型增生,n = 5)也进行了检查。Kaplan-Meier分析显示LAT 1-高和-低评分在PDAC中存在显著差异。即使在每个Ki-67标记指数(LI)低和高PDAC组(截断值40%)中,LAT 1高表达也可预测不良预后。多因素分析显示LAT 1表达、Ki-67 LI、肿瘤分化程度和肿瘤大小是影响PDAC患者预后的独立因素。结论LAT 1在PDAC中的异常过表达与Ki-67 LI无关,提示PDAC患者预后不良,LAT 1抑制剂可作为今后抗肿瘤治疗的潜在靶点。
Background and aims Molecular target therapy against L-type amino acid transporter 1 (LAT1) is unique and expected to be developed soon. LAT1 expression was investigated in pancreatic cancer as a prognostic predictor.Methods Surgically resected pancreatic ductal adenocarcinomas (PDAC, n = 66) were investigated using immunohistochemistry. For reference, intraductal papillary mucinous carcinomas (IPMC, including intraductal papillary mucinous neoplasm (IPMN) with high-grade dysplasia or with an associated invasive carcinoma, n = 13) and adenomas (IPMA, including IPMN with low- and intermediate-grade dysplasia, n = 5) were also examined.Results LAT1 expression scores increased from PDAC to IPMA to IPMC. Kaplan-Meier analysis showed significant differences between LAT1-high and -low scores in PDAC. Even in each Ki-67-labelling index (LI) low and high PDAC group (cut off 40%), high LAT1 expression could also predict poor prognosis. Multivariable analysis showed that LAT1 expression, Ki-67 LI, tumour differentiation and size were individual prognostic factors.Conclusions LAT1 aberrant overexpression in PDAC predicts poor prognosis, independent of Ki-67 LI, and offers a potential target for future anticancer therapy with its inhibitors.