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
. 2002;19(7):603-8.
doi: 10.1023/a:1020950420196.

Expression of autotaxin (NPP-2) is closely linked to invasiveness of breast cancer cells

Affiliations

Expression of autotaxin (NPP-2) is closely linked to invasiveness of breast cancer cells

So Young Yang et al. Clin Exp Metastasis. 2002.

Abstract

Autotaxin (ATX), originally isolated from human melanoma cells, is a novel metastasis-enhancing motogen and angiogenesis factor. In the present study, we compared the expression level of ATX mRNA between normal and breast cancer tissues and found that the expression of ATX mRNA was closely linked to invasiveness of cancer cells. Reverse transcriptase-polymerase chain reaction (RT-PCR) and immunohistochemical analysis showed higher cellular ATX mRNA expression in the cancer than normal breast tissues. MDA-MB-435S breast cancer cells, expressing higher amount of ATX mRNA, showed greater relative invasiveness to fibroblast-conditioned medium (FCM) than MCF7, MDA-MB-231, and HBL-100 breast cancer cells. Furthermore, ATX-transfected MCF7 cells showed increased motility and invasiveness than vector-transfected MCF7 cells. Collectively, our results suggest that the expression of ATX is closely linked to the invasiveness of breast cancer cells.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Annu Rev Cell Biol. 1986;2:337-65 - PubMed
    1. J Biol Chem. 1990 Oct 15;265(29):17506-11 - PubMed
    1. J Biol Chem. 1995 Apr 28;270(17):9849-55 - PubMed
    1. Am J Respir Cell Mol Biol. 1999 Aug;21(2):216-22 - PubMed
    1. J Biol Chem. 1996 Oct 11;271(41):25107-16 - PubMed

Publication types

MeSH terms

Substances