The plasma membrane transporter SLC5A8 can inhibit the spread of tumours
by decreasing the amount of the anti-apoptotic protein surviving in
tumour cells.
Tumour cells need far more nutrients that normal cells and these
nutrients cannot get into the malignant cells without transporters.
These are compounds that are responsible for the absorption of
peptides, amino acids, sugars, vitamins and other nutrients. They exist
in all cell types, particularly in those tissues responsible for the
absorption of nutrients, such as the intestine and kidneys.
What if you could turn off a transporter that was important to tumour cells, but not to normal cells?
Dr Vadivel Ganapathy, of the Medical College of Georgia, suggests we
can do that. He and his team report in a paper published in the Biochemical Journal
on January 24 that the plasma membrane transporter SLC5A8 can inhibit
the spread of tumours by decreasing the amount of the anti-apoptotic
protein surviving in tumour cells. This induces apoptosis (cell death)
and renders the tumour cells more sensitive to anti-cancer drugs. All
this without affecting the activity of SLC5A8 in normal cells.
Tests in breast cancer cells in mice have proved promising. "Our
studies unravel a novel, hitherto unrecognized, mechanism for the
tumour-suppressive role of a plasma membrane transporter independent of
its transport function," he says.
Journal Reference:
- Veena Coothankandaswamy, Selvakumar Elangovan, Nagendra Singh, Puttur D. Prasad, Muthusamy Thangaraju, Vadivel Ganapathy. The plasma membrane transporter SLC5A8 suppresses tumour progression through depletion of survivin without involving its transport function. Biochemical Journal, 2013; 450 (1): 169 DOI: 10.1042/BJ20121248
Courtesy: ScienceDaily
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