Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 Nov;14(5):5077-5084.
doi: 10.3892/ol.2017.6882. Epub 2017 Sep 4.

Role of galectins in lung cancer

Affiliations

Role of galectins in lung cancer

Wei-An Chang et al. Oncol Lett. 2017 Nov.

Abstract

Lung cancer is the leading cause of cancer-associated mortality worldwide and is also associated with a poor prognosis. As in numerous other types of cancer, galectins have been demonstrated to be involved in the progression of lung cancer. Galectins belong to a superfamily of lectins, which are carbohydrate-binding proteins. There are at least 15 members in the galectin family, however, only galectin-1, -2, -3, -4, -7, -8, -9, -10, -12, and -13 are found in humans. Galectins are able to mediate interactions between cells, including homotypic and heterotypic interactions; they also facilitate the bindings between cells and extracellular matrix components. These cell-cell and cell-matrix interactions, as well as the galectin signaling on the cell surface, are able to modulate signaling pathways and thereby influence cellular functions and behaviors. Galectin-1, -3, -4, -7, -8 and -9 are associated with lung cancer. These galectins are associated with tumor invasion, migration, metastasis and progression, and may serve important roles in the tumor microenvironment of lung cancer. The majority of galectins are associated with the progression of lung cancer, with the exception of galectin-9, which is associated with enhanced anticancer immunity. Therefore, galectins may be potential targets for developing novel lung cancer therapies.

Keywords: galectin; lung cancer; malignancy; tumor microenvironment.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Classification of galectins into prototypical (dimeric), tandem-repeat and chimeric galectins. Prototypical (dimeric) galectins possess two identical CRDs. Tandem-repeat galectins possess two distinct CRDs. Chimeric galectins possess a single CRD, and may aggregate to form its common appearance with multiple identical CRDs. CRD, carbohydrate-recognition domains.
Figure 2.
Figure 2.
Galectins are able to mediate cell-cell and cell-matrix interactions, and thereby modulate signaling pathways and influence cellular behavior.
Figure 3.
Figure 3.
Roles of galectins in lung cancer. Galectins affect the progression of lung cancer in multiple aspects, including tumor migration, tumor progression, metastasis, tumor invasion, drug resistance, sphere-formation and the interactions between cells in the tumor microenvironment.

Similar articles

Cited by

References

    1. Barondes SH, Cooper DN, Gitt MA, Leffler H. Galectins. Structure and function of a large family of animal lectins. J Biol Chem. 1994;269:20807–20810. - PubMed
    1. Powell JT, Whitney PL. Postnatal development of rat lung. Changes in lung lectin, elastin, acetylcholinesterase and other enzymes. Biochem J. 1980;188:1–8. doi: 10.1042/bj1880001. - DOI - PMC - PubMed
    1. Buttery R, Monaghan H, Salter DM, Sethi T. Galectin-3: Differential expression between small-cell and non-small-cell lung cancer. Histopathology. 2004;44:339–344. doi: 10.1111/j.1365-2559.2004.01815.x. - DOI - PubMed
    1. Cummings RD, Liu FT. Chapter 33 Galectins. In: Varki A, Cummings RD, Esko JD, et al., editors. Essentials of Glycobiology. 2nd edition. Cold Spring Harbor Laboratory Press; La Jolla, California: 2009.
    1. Hsu YL, Wu CY, Hung JY, Lin YS, Huang MS, Kuo PL. Galectin-1 promotes lung cancer tumor metastasis by potentiating integrin α6β4 and Notch1/Jagged2 signaling pathway. Carcinogenesis. 2013;34:1370–1381. doi: 10.1093/carcin/bgt040. - DOI - PubMed