» Articles » PMID: 21548930

Loss of Aquaporin-4 Expression and Putative Function in Non-small Cell Lung Cancer

Overview
Journal BMC Cancer
Publisher Biomed Central
Specialty Oncology
Date 2011 May 10
PMID 21548930
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Aquaporins (AQPs) have been recognized to promote tumor progression, invasion, and metastasis and are therefore recognized as promising targets for novel anti-cancer therapies. Potentially relevant AQPs in distinct cancer entities can be determined by a comprehensive expression analysis of the 13 human AQPs.

Methods: We analyzed the presence of all AQP transcripts in 576 different normal lung and non-small cell lung cancer (NSCLC) samples using microarray data and validated our findings by qRT-PCR and immunohistochemistry.

Results: Variable expression of several AQPs (AQP1, -3, -4, and -5) was found in NSCLC and normal lung tissues. Furthermore, we identified remarkable differences between NSCLC subtypes in regard to AQP1, -3 and -4 expression. Higher transcript and protein levels of AQP4 in well-differentiated lung adenocarcinomas suggested an association with a more favourable prognosis. Beyond water transport, data mining of co-expressed genes indicated an involvement of AQP4 in cell-cell signalling, cellular movement and lipid metabolism, and underlined the association of AQP4 to important physiological functions in benign lung tissue.

Conclusions: Our findings accentuate the need to identify functional differences and redundancies of active AQPs in normal and tumor cells in order to assess their value as promising drug targets.

Citing Articles

Important functions and molecular mechanisms of aquaporins family on respiratory diseases: potential translational values.

Li J, Yang D, Lin L, Yu L, Chen L, Lu K J Cancer. 2024; 15(18):6073-6085.

PMID: 39440058 PMC: 11493008. DOI: 10.7150/jca.98829.


Alveolar-Capillary Barrier Protection In Vitro: Lung Cell Type-Specific Effects and Molecular Mechanisms Induced by 1α, 25-Dihydroxyvitamin D3.

Xiong J, Kaleja P, Uckert L, Nezaratizadeh N, Krantz S, Krause M Int J Mol Sci. 2023; 24(8).

PMID: 37108455 PMC: 10138495. DOI: 10.3390/ijms24087298.


Relevant Membrane Transport Proteins as Possible Gatekeepers for Effective Pharmacological Ascorbate Treatment in Cancer.

Leischner C, Marongiu L, Piotrowsky A, Niessner H, Venturelli S, Burkard M Antioxidants (Basel). 2023; 12(4).

PMID: 37107291 PMC: 10135768. DOI: 10.3390/antiox12040916.


The Role of Aquaporin 5 (AQP5) in Lung Adenocarcinoma: A Review Article.

Jaskiewicz L, Romaszko-Wojtowicz A, Doboszynska A, Skowronska A Cells. 2023; 12(3).

PMID: 36766810 PMC: 9913646. DOI: 10.3390/cells12030468.


Aquaporins in Respiratory System.

Wang L, Wang J, Zhu X, Bai C, Song Y Adv Exp Med Biol. 2023; 1398:137-144.

PMID: 36717491 DOI: 10.1007/978-981-19-7415-1_9.


References
1.
Monzani E, Shtil A, La Porta C . The water channels, new druggable targets to combat cancer cell survival, invasiveness and metastasis. Curr Drug Targets. 2007; 8(10):1132-7. DOI: 10.2174/138945007782151342. View

2.
Rojek A, Praetorius J, Frokiaer J, Nielsen S, Fenton R . A current view of the mammalian aquaglyceroporins. Annu Rev Physiol. 2007; 70:301-27. DOI: 10.1146/annurev.physiol.70.113006.100452. View

3.
Wang I, Meliton L, Tretiakova M, Costa R, Kalinichenko V, Kalin T . Transgenic expression of the forkhead box M1 transcription factor induces formation of lung tumors. Oncogene. 2008; 27(30):4137-49. DOI: 10.1038/onc.2008.60. View

4.
Xu H, Zhang Y, Wei W, Shen L, Wu W . Differential expression of aquaporin-4 in human gastric normal and cancer tissues. Gastroenterol Clin Biol. 2008; 33(1 Pt 1):72-6. DOI: 10.1016/j.gcb.2008.07.010. View

5.
Liu Y, Matsuzaki T, Nakazawa T, Murata S, Nakamura N, Kondo T . Expression of aquaporin 3 (AQP3) in normal and neoplastic lung tissues. Hum Pathol. 2006; 38(1):171-8. DOI: 10.1016/j.humpath.2006.07.015. View