• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

V-ATPase 的表达与非小细胞肺癌的耐药性和病理学有关。

The expression of V-ATPase is associated with drug resistance and pathology of non-small-cell lung cancer.

机构信息

Department of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, 710038 Xi'an, PR China.

出版信息

Diagn Pathol. 2013 Aug 28;8:145. doi: 10.1186/1746-1596-8-145.

DOI:10.1186/1746-1596-8-145
PMID:23984887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3846167/
Abstract

OBJECTIVE

This article aims to investigate the expression of vacuolar-H + -ATPase (V-ATPase) in non-small cell lung cancer (NSCLC) and its variations with pathological type and grade. Furthermore, to evaluate the chemotherapy drug sensitivity of different cancer tissues as well as its correlation with V-ATPase expression in NSCLC.

METHODS

V-ATPase expression was examined in 92 NSCLC tissue samples using the immunohistochemical Envision method and immunofluorescence assay. The location of V-ATPase expression was observed by confocal laser scanning microscopy and the difference of its expression rate was evaluated. The sensitivity of cancer tissues to chemotherapy drug was examined using MTT assay and its correlation with the V-ATPase expression was tested in NSCLC by Spearman rank correlation analysis.

RESULTS

V-ATPase expression was mainly localized in the cell membrane and cytoplasm. The expression rate of V-ATPase was 71.43% in squamous cell lung cancer, significantly lower than that of the lung adenocarcinoma (83.72%, P = 0.000). In different pathological grades of squamous cell lung cancer, the expression rate of V-ATPase was 58.33% in grade II, significantly lower than that of the grade III (84.00%, P = 0.014). The expression rate of V-ATPase in grade II lung adenocarcinoma was 76.67%, significantly lower than that of the grade ΙΙΙ adenocarcinoma (100.0%, P = 0.012). Correlation analysis showed that the sensitivity of NSCLC tissues to cyclophosphamide, gemcitabine, doxorubicin, paclitaxel and cisplatin was significantly correlated with the V-ATPase expression rate (P < 0.05).

CONCLUSIONS

V-ATPase was overexpressed in NSCLC. The expression of V-ATPase was related to the pathological type and grade of cancer and was likely associated with chemotherapy drug resistance in NSCLC.

VIRTUAL SLIDES

The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/7515811511020000.

摘要

目的

本文旨在研究空泡质子泵(V-ATPase)在非小细胞肺癌(NSCLC)中的表达及其与病理类型和分级的变化。此外,评估不同癌组织的化疗药物敏感性及其与 NSCLC 中 V-ATPase 表达的相关性。

方法

采用免疫组织化学 Envision 法和免疫荧光法检测 92 例 NSCLC 组织中 V-ATPase 的表达,应用共聚焦激光扫描显微镜观察 V-ATPase 的表达部位,评估其表达率的差异。采用 MTT 法检测癌组织对化疗药物的敏感性,并采用 Spearman 秩相关分析检测 NSCLC 中 V-ATPase 表达与化疗药物敏感性的相关性。

结果

V-ATPase 主要定位于细胞膜和细胞质。V-ATPase 在鳞癌中的表达率为 71.43%,明显低于肺腺癌(83.72%,P=0.000)。在不同病理分级的鳞癌中,V-ATPase 在Ⅱ级的表达率为 58.33%,明显低于Ⅲ级(84.00%,P=0.014)。Ⅱ级肺腺癌中 V-ATPase 的表达率为 76.67%,明显低于Ⅲ级腺癌(100.0%,P=0.012)。相关性分析显示,NSCLC 组织对环磷酰胺、吉西他滨、阿霉素、紫杉醇和顺铂的敏感性与 V-ATPase 表达率呈显著相关(P<0.05)。

结论

V-ATPase 在 NSCLC 中过度表达。V-ATPase 的表达与癌症的病理类型和分级有关,可能与 NSCLC 化疗耐药有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f49/3846167/f10400589fcb/1746-1596-8-145-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f49/3846167/25871985b6d8/1746-1596-8-145-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f49/3846167/f10400589fcb/1746-1596-8-145-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f49/3846167/25871985b6d8/1746-1596-8-145-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f49/3846167/f10400589fcb/1746-1596-8-145-2.jpg

相似文献

1
The expression of V-ATPase is associated with drug resistance and pathology of non-small-cell lung cancer.V-ATPase 的表达与非小细胞肺癌的耐药性和病理学有关。
Diagn Pathol. 2013 Aug 28;8:145. doi: 10.1186/1746-1596-8-145.
2
ABCG2/V-ATPase was associated with the drug resistance and tumor metastasis of esophageal squamous cancer cells.ABCG2/V-ATPase 与食管鳞癌细胞的耐药性和肿瘤转移有关。
Diagn Pathol. 2012 Dec 17;7:180. doi: 10.1186/1746-1596-7-180.
3
Methionine Aminopeptidase 2 as a Potential Therapeutic Target for Human Non-Small-Cell Lung Cancers.蛋氨酸氨肽酶2作为人类非小细胞肺癌的潜在治疗靶点
Adv Clin Exp Med. 2016 Jan-Feb;25(1):117-28. doi: 10.17219/acem/60715.
4
[The expression of ABCG4, V-ATPase and clinic significance of their correlation with NSCLC.].[ABCG4、V-ATP酶的表达及其与非小细胞肺癌相关性的临床意义。]
Zhongguo Fei Ai Za Zhi. 2008 Oct 20;11(5):691-5. doi: 10.3779/j.issn.1009-3419.2008.05.023.
5
Distinct prognostic values and potential drug targets of ALDH1 isoenzymes in non-small-cell lung cancer.醛脱氢酶1同工酶在非小细胞肺癌中的不同预后价值及潜在药物靶点
Drug Des Devel Ther. 2015 Sep 3;9:5087-97. doi: 10.2147/DDDT.S87197. eCollection 2015.
6
Correlation between chemosensitivity to anticancer drugs and telomerase reverse transcriptase mRNA expression in gastric cancer.胃癌中抗癌药物的化疗敏感性与端粒酶逆转录酶 mRNA 表达的相关性。
Diagn Pathol. 2013 Feb 22;8:33. doi: 10.1186/1746-1596-8-33.
7
High expression of Rad51c predicts poor prognostic outcome and induces cell resistance to cisplatin and radiation in non-small cell lung cancer.Rad51c的高表达预示着非小细胞肺癌患者预后不良,并诱导细胞对顺铂和放疗产生抗性。
Tumour Biol. 2016 Oct;37(10):13489-13498. doi: 10.1007/s13277-016-5192-x. Epub 2016 Jul 27.
8
Expression of SIRT1 and cortactin is associated with progression of non-small cell lung cancer.SIRT1 和 cortactin 的表达与非小细胞肺癌的进展相关。
Pathol Res Pract. 2013 Jun;209(6):365-70. doi: 10.1016/j.prp.2013.03.011. Epub 2013 Apr 15.
9
Overexpression of CHD1L is positively associated with metastasis of lung adenocarcinoma and predicts patients poor survival.CHD1L的过表达与肺腺癌转移呈正相关,并预示患者预后不良。
Oncotarget. 2015 Oct 13;6(31):31181-90. doi: 10.18632/oncotarget.5070.
10
Limited Clinical Significance of Dimeric Form of Pyruvate Kinase as a Diagnostic and Prognostic Biomarker in Non-small Cell Lung Cancer.丙酮酸激酶二聚体形式作为非小细胞肺癌诊断和预后生物标志物的临床意义有限。
Adv Exp Med Biol. 2017;955:51-57. doi: 10.1007/5584_2016_92.

引用本文的文献

1
Ex vivo drug responses and molecular profiles of 597 pediatric acute lymphoblastic leukemia patients.597例儿童急性淋巴细胞白血病患者的体外药物反应及分子特征
Hemasphere. 2025 Jul 28;9(7):e70176. doi: 10.1002/hem3.70176. eCollection 2025 Jul.
2
The Role of V-ATPase ATP6V0D1 Subunit in Chemoresistance and Ellipticine-Induced Cytoplasmic Vacuolation in Neuroblastoma Cells.V-ATP酶ATP6V0D1亚基在神经母细胞瘤细胞化疗耐药及椭圆玫瑰树碱诱导的细胞质空泡化中的作用
Mol Cell Oncol. 2025 Jun 17;12(1):2518774. doi: 10.1080/23723556.2025.2518774. eCollection 2025.
3
Antitumor and immunomodulatory activities of diphyllin and its derivatives.

本文引用的文献

1
Aeluropus littoralis NaCl-induced vacuolar H(+)-ATPase subunit c: molecular cloning and expression analysis.盐胁迫下獐毛液泡H(+) -ATP酶亚基c的克隆与表达分析
Genetika. 2012 Dec;48(12):1380-8.
2
Cold stress causes rapid but differential changes in properties of plasma membrane H(+)-ATPase of camelina and rapeseed.冷应激导致荠蓝和油菜细胞质膜 H(+)-ATP 酶性质的快速但有差异的变化。
J Plant Physiol. 2013 Jun 15;170(9):828-37. doi: 10.1016/j.jplph.2013.01.007. Epub 2013 Feb 8.
3
Vacuolar H+ ATPase expression and activity is required for Rab27B-dependent invasive growth and metastasis of breast cancer.
双叶豆素及其衍生物的抗肿瘤和免疫调节活性。
Bioorg Med Chem. 2025 Jul 1;124:118197. doi: 10.1016/j.bmc.2025.118197. Epub 2025 Apr 14.
4
V-ATPase in glioma stem cells: a novel metabolic vulnerability.胶质瘤干细胞中的V-ATP酶:一种新的代谢脆弱性。
J Exp Clin Cancer Res. 2025 Jan 17;44(1):17. doi: 10.1186/s13046-025-03280-3.
5
Identification of ATP6V0A4 as a potential biomarker in renal cell carcinoma using integrated bioinformatics analysis.通过综合生物信息学分析鉴定ATP6V0A4作为肾细胞癌的潜在生物标志物
Oncol Lett. 2023 Jul 11;26(3):366. doi: 10.3892/ol.2023.13952. eCollection 2023 Sep.
6
Resistance to Chemotherapeutic 5-Fluorouracil Conferred by Modulation of Heterochromatic Integrity through Ino80 Function in Fission Yeast.通过 Ino80 功能调节异染色质完整性对裂殖酵母中化疗药物 5-氟尿嘧啶的耐药性。
Int J Mol Sci. 2023 Jun 26;24(13):10687. doi: 10.3390/ijms241310687.
7
Factor-specific generative pattern from large-scale drug-induced gene expression profile.基于大规模药物诱导基因表达谱的因子特异性生成模式。
Sci Rep. 2023 Apr 18;13(1):6339. doi: 10.1038/s41598-023-33061-x.
8
High ATP6V1B1 expression is associated with poor prognosis and platinum‑based chemotherapy resistance in epithelial ovarian cancer.ATP6V1B1 高表达与上皮性卵巢癌不良预后和铂类化疗耐药相关。
Oncol Rep. 2023 May;49(5). doi: 10.3892/or.2023.8539. Epub 2023 Mar 31.
9
A Multi-Omics Network of a Seven-Gene Prognostic Signature for Non-Small Cell Lung Cancer.一个包含七个基因预后标志物的非小细胞肺癌多组学网络。
Int J Mol Sci. 2021 Dec 25;23(1):219. doi: 10.3390/ijms23010219.
10
Crosstalk between autophagy inhibitors and endosome-related secretory pathways: a challenge for autophagy-based treatment of solid cancers.自噬抑制剂与内体相关分泌途径的串扰:基于自噬治疗实体瘤的挑战。
Mol Cancer. 2021 Oct 27;20(1):140. doi: 10.1186/s12943-021-01423-6.
液泡型 H+ 三磷酸腺苷酶的表达和活性是乳腺癌 Rab27B 依赖性浸润生长和转移所必需的。
Int J Cancer. 2013 Aug 15;133(4):843-54. doi: 10.1002/ijc.28079. Epub 2013 Mar 7.
4
ABCG2/V-ATPase was associated with the drug resistance and tumor metastasis of esophageal squamous cancer cells.ABCG2/V-ATPase 与食管鳞癌细胞的耐药性和肿瘤转移有关。
Diagn Pathol. 2012 Dec 17;7:180. doi: 10.1186/1746-1596-7-180.
5
Tonoplast calcium sensors CBL2 and CBL3 control plant growth and ion homeostasis through regulating V-ATPase activity in Arabidopsis.液泡膜钙传感器 CBL2 和 CBL3 通过调节拟南芥 V-ATPase 活性控制植物生长和离子稳态。
Cell Res. 2012 Dec;22(12):1650-65. doi: 10.1038/cr.2012.161. Epub 2012 Nov 27.
6
Molecular modeling and description of a newly characterized activating mutation of the EGFR gene in non-small cell lung cancer.非小细胞肺癌中新型 EGFR 基因激活突变的分子建模与描述。
Diagn Pathol. 2012 Oct 22;7:146. doi: 10.1186/1746-1596-7-146.
7
The V-ATPase-inhibitor archazolid abrogates tumor metastasis via inhibition of endocytic activation of the Rho-GTPase Rac1.V-ATPase 抑制剂 archazolid 通过抑制 Rho-GTPase Rac1 的内吞激活来阻断肿瘤转移。
Cancer Res. 2012 Nov 15;72(22):5976-87. doi: 10.1158/0008-5472.CAN-12-1772. Epub 2012 Sep 17.
8
Lung cancers with acquired resistance to EGFR inhibitors occasionally harbor BRAF gene mutations but lack mutations in KRAS, NRAS, or MEK1.具有获得性 EGFR 抑制剂耐药的肺癌偶尔会发生 BRAF 基因突变,但缺乏 KRAS、NRAS 或 MEK1 突变。
Proc Natl Acad Sci U S A. 2012 Jul 31;109(31):E2127-33. doi: 10.1073/pnas.1203530109. Epub 2012 Jul 6.
9
A systematic analysis of efficacy of second-line chemotherapy in sensitive and refractory small-cell lung cancer.二线化疗在敏感和难治性小细胞肺癌中的疗效的系统分析。
J Thorac Oncol. 2012 May;7(5):866-72. doi: 10.1097/JTO.0b013e31824c7f4b.
10
A comprehensive study of polymorphisms in ABCB1, ABCC2 and ABCG2 and lung cancer chemotherapy response and prognosis.多态性在 ABCB1、ABCC2 和 ABCG2 与肺癌化疗反应和预后的综合研究。
Int J Cancer. 2012 Dec 15;131(12):2920-8. doi: 10.1002/ijc.27567. Epub 2012 Jul 3.