Aquaporin 1 is overexpressed in lung cancer and stimulates NIH-3T3 cell proliferation and anchorage-independent growth

被引:181
|
作者
Hoque, MO
Soria, JC
Woo, JH
Lee, T
Lee, J
Jang, SJ
Upadhyay, S
Trink, B
Monitto, C
Desmaze, C
Mao, L
Sidransky, D
Moon, C
机构
[1] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Sch Med, Dept Anesthesiol & Crit Care Med, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21218 USA
[5] Univ Texas, MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Mol Biol Lab, Houston, TX 77030 USA
[6] Inst Gustave Roussy, Div Canc Med, Villejuif, France
[7] Univ Ulsan, Coll Med, Asan Med Coll, Dept Pathol, Seoul, South Korea
来源
AMERICAN JOURNAL OF PATHOLOGY | 2006年 / 168卷 / 04期
关键词
D O I
10.2353/ajpath.2006.050596
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The aquaporins represent a family of transmembrane water channel proteins that play a major role in transcellular and transepithelial water movement. Most tumors have been shown to exhibit high vascular permeability and interstitial fluid pressure, but the transport pathways for water within tumors remain unknown. Here, we tested 10 non-small cell lung cancer cell lines of various origins by reverse transcriptase-polymerase chain reaction and Western blot analysis and identified clear expression of aquaporin 1 (AQP1) in seven cell lines. We next examined the distribution of the AQP1 protein in several types of primary lung tumors (16 squamous cell carcinomas, 21 adenocarcinomas, and 7 bronchoalveolar carcinomas) by immunohistochemical staining. AQP1 was overexpressed in 62% (13 of 21) and 75% (6 of 8) of adenocarcinoma and bronchoalveolar carcinoma, respectivelv, whereas all cases of squamous cell carcinoma and normal lung tissue were negative. Forced expression of full-length AQP1 cDNA in NIH-3T3 cells induced many phenotypic changes characteristic of transformation, including cell proliferation-enhancing activity by the MTT assay and anchorage-independent growth in soft agar. Although further details on the molecular function of AQP1 related to tumorigenesis remain to be elucidated, our results suggest a potential role of AQP1 as a novel therapeutic target for the management of lung cancer.
引用
收藏
页码:1345 / 1353
页数:9
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