Suppr超能文献

GADD153表达在I期非小细胞肺癌中的临床意义

Clinical significance of GADD153 expression in stage I non-small cell lung cancer.

作者信息

Lee Chang Youl, Lee Myung Goo, Choi Kyung Chan, Kang Hee Mo, Chang Yoon Soo

机构信息

Department of Internal Medicine, Chuncheon Sacred Heart Hospital, Hallym University Medical Center, Seoul 135-720, Republic of Korea.

出版信息

Oncol Lett. 2012 Sep;4(3):408-412. doi: 10.3892/ol.2012.768. Epub 2012 Jun 21.

Abstract

The transcription factor growth arrest and DNA damage-inducible gene 153 (GADD153), also known as CHOP, is considered to function as a proapoptotic molecule. Overexpression of GADD153 leads to cell cycle arrest and/or apoptosis. However, its clinical implications in non-small cell lung cancer (NSCLC) remain controversial. Therefore, we investigated the expression of GADD153 in stage I NSCLC using immunohistochemistry. Paraffin-embedded tissue sections from 76 patients, who were diagnosed with primary stage I NSCLC and had undergone a curative lung resection, were stained using an anti-GADD153 antibody. The intensity of GADD153 immunostaining was evaluated within the cell membrane and cytoplasm of invasive cancer components. The correlation between the intratumoral expression of GADD153 and various clinical parameters were explored. GADD153 was detected in 29 (38.2%) cases. No statistically significant difference in expression was demonstrated between stage IA and stage IB tumors (35.0 vs. 39.3%; P=0.735). The expression of GADD153 was not affected by histological subtypes or histological grades of differentiation. The intratumoral expression of GADD153 did not influence the overall survival rate (53.29 vs. 52.18 months; P=0.743) or disease-free survival rate (46.97 vs. 54.19 months; P=0.084) of stage I NSCLC patients. However, patients with GADD153 expression demonstrated an improved disease-specific survival rate (28.80 vs. 53.85 months; P=0.020). No patients with GADD153 expression demonstrated distant metastasis (P=0.029). These data suggest that GADD153 expression may be a valuable prognostic factor of early-stage NSCLC in patients who have undergone curative lung resection.

摘要

转录因子生长停滞和DNA损伤诱导基因153(GADD153),也称为CHOP,被认为是一种促凋亡分子。GADD153的过表达导致细胞周期停滞和/或凋亡。然而,其在非小细胞肺癌(NSCLC)中的临床意义仍存在争议。因此,我们使用免疫组织化学方法研究了GADD153在I期NSCLC中的表达。对76例被诊断为原发性I期NSCLC并接受了根治性肺切除术的患者的石蜡包埋组织切片,用抗GADD153抗体进行染色。在浸润性癌成分的细胞膜和细胞质内评估GADD153免疫染色的强度。探讨了GADD153肿瘤内表达与各种临床参数之间的相关性。在29例(38.2%)病例中检测到GADD153。IA期和IB期肿瘤之间的表达无统计学显著差异(35.0%对39.3%;P = 0.735)。GADD153的表达不受组织学亚型或组织学分化程度的影响。GADD153的肿瘤内表达不影响I期NSCLC患者的总生存率(53.29个月对52.18个月;P = 0.743)或无病生存率(46.97个月对54.19个月;P = 0.084)。然而,有GADD153表达的患者疾病特异性生存率有所提高(28.80个月对53.85个月;P = 0.020)。有GADD153表达的患者均未发生远处转移(P = 0.029)。这些数据表明,GADD153表达可能是接受了根治性肺切除术的早期NSCLC患者的一个有价值的预后因素。

相似文献

1
Clinical significance of GADD153 expression in stage I non-small cell lung cancer.
Oncol Lett. 2012 Sep;4(3):408-412. doi: 10.3892/ol.2012.768. Epub 2012 Jun 21.
8
Relationship between CHOP/GADD153 and unstable human carotid atherosclerotic plaque.
Br J Neurosurg. 2017 Dec;31(6):648-652. doi: 10.1080/02688697.2017.1327016. Epub 2017 May 17.
10

引用本文的文献

2
Effects of ambient PM and 9-nitroanthracene on DNA damage and repair, oxidative stress and metabolic enzymes in the lungs of rats.
Toxicol Res (Camb). 2017 May 18;6(5):654-663. doi: 10.1039/c7tx00065k. eCollection 2017 Sep 1.
3
HSP90B1 overexpression predicts poor prognosis in NSCLC patients.
Tumour Biol. 2016 Oct;37(10):14321-14328. doi: 10.1007/s13277-016-5304-7. Epub 2016 Sep 6.
4
Elucidation of a novel phenformin derivative on glucose-deprived stress responses in HT-29 cells.
Mol Cell Biochem. 2016 Aug;419(1-2):29-40. doi: 10.1007/s11010-016-2747-5. Epub 2016 Jul 8.
5
Pazopanib diminishes non-small cell lung cancer (NSCLC) growth and metastases in vivo.
Thorac Cancer. 2015 Mar;6(2):133-40. doi: 10.1111/1759-7714.12138. Epub 2015 Mar 2.

本文引用的文献

1
Expression of ER stress and autophagy-related molecules in human non-small cell lung cancer and premalignant lesions.
Int J Cancer. 2012 Aug 15;131(4):E362-70. doi: 10.1002/ijc.26463. Epub 2011 Nov 9.
2
Cancer statistics, 2010.
CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300. doi: 10.3322/caac.20073. Epub 2010 Jul 7.
3
ER stress triggers apoptosis by activating BH3-only protein Bim.
Cell. 2007 Jun 29;129(7):1337-49. doi: 10.1016/j.cell.2007.04.027.
7
Increased GADD gene expression in human colon epithelial cells exposed to deoxycholate.
J Cell Physiol. 2005 Jan;202(1):295-303. doi: 10.1002/jcp.20135.
8
Roles of CHOP/GADD153 in endoplasmic reticulum stress.
Cell Death Differ. 2004 Apr;11(4):381-9. doi: 10.1038/sj.cdd.4401373.
9
The dark side of Ras: regulation of apoptosis.
Oncogene. 2003 Dec 8;22(56):8999-9006. doi: 10.1038/sj.onc.1207111.
10
Targeting RAS signalling pathways in cancer therapy.
Nat Rev Cancer. 2003 Jan;3(1):11-22. doi: 10.1038/nrc969.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验