| Painkiller's
Ulcerous Trail
HST-1 helps manage
side-effects of cancer treatmentAN ANTIOXIDANT called resveratrol,
found in plants like grapes, peanuts, spruce, lily and mulberries,
is known to be a good anticancer agent but it decelerates
ulcer healing. Cancer patients are given pain killers that
cause ulcers as side-effects. Hence resveratrol cannot be
given to cancer patients with gastric ulcers. To do away with
this limitation, a research team from Kolkata has synthesized
a novel anti-cancer compound that is structurally similar
to resveratrol and does not disrupt the ulcer healing process.
A team led by
researchers from Kolkata's B C Roy Institute of Basic Medical
Sciences and Institute of Post Graduate Medical Education
and Research, Anthropological Survey of India and Bio-Organic
Division at the Bhabha Atomic Research Centre, Mumbai, synthesized
several substances structurally similar to resveratrol. While
doing it, they hit upon a novel compound called HST-1. This
drug inhibited the growth of two types of human blood cancer
cells and didn't have the drawback of resveratrol.
To test the efficacy
of HST-1 against ulcers, the researchers fed mice with indomethacin,
a non-steroidal anti-inflammatory painkiller, to cause ulcers
in their stomachs. These mice then received either resveratrol
or HST-1 and were compared with ulcerated untreated mice.
"HST-1 accelerated
the healing of the ulcers along with showing strong anticancer
properties similar to that of resveratrol," said lead
researcher Sandip K Bandyopadhyay. In an ulcerated condition,
the activity of the enzyme myeloperoxidase (MPO) increases
at the site of inflammation, blocking the healing process.
There was a marked reduction in the activity of MPO in HST-1
treated mice compared to the ulcerated untreated and resveratrol-treated
mice, confirming its ulcer-healing potency. They found that
resveratrol also suppressed the activity of cyclooxygenase-1
(COX-1), an enzyme that aids in the synthesis of prostaglandin
E2 which protects the inner lining of the stomach from acid
attack. HST-1 did not inhibit the activity of COX-1.
The researchers
exposed HST-1 and resveratrol to cultured cells of two types
of human blood cancers for two days. When it came to driving
the cancer cells to commit mass suicide, HST-1 proved more
effective than resveratrol. The study was published in the
December 9 issue of Journal of Pharmacology And Experimental
Therapeutics.
Source: Down
To Earth,
Date:
February, 2009

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