Vitamin A may turn back the clock on breast cancer
A
derivative of vitamin A, known as retinoic acid, found abundantly in sweet
potato and carrots, helps turn pre-cancer cells back to normal healthy breast
cells, a new study has found.
The
research could help explain why some clinical studies have been unable to see a
benefit of vitamin A on cancer: the vitamin does not appear to change the
course of full-blown cancer, only pre-cancerous cells, and only works at a very
narrow dose.
Since
cells undergo many changes before they become fully aggressive and metastatic,
Sandra V Fernandez, Assistant Research Professor of Medical Oncology at Thomas
Jefferson University, and colleagues, used a model of breast cancer progression
composed of four types of cells each one representing a different stage of
breast cancer: normal, pre-cancerous, cancerous and a fully aggressive model.
When
the researchers exposed the four breast cell types to different concentrations
of retinoic acid - one of the chemicals that the body converts vitamin A into -
they noticed a strong change in the pre-cancerous cells.
Not
only did the pre-cancerous cells begin to look more like normal cells in terms
of their shape, they also changed their genetic signature back to normal.
The
pre-cancerous cells had 443 genes that were either up or downregulated on their
way to becoming cancerous. All of these genes returned to normal levels after
treatment with retinoic acid.
"It
looks like retinoic acid exerts effects on cancer cells in part via the
modulation of the epigenome," said Fernandez.
"We
were able to see this effect of retinoic acid because we were looking at four
distinct stages of breast cancer. It will be interesting to see if these
results can be applied to patients," said Fernandez.
The
cells that were considered fully cancerous did not respond at all to retinoic
acid, suggesting that there may be a small window of opportunity for retinoic
acid to be helpful in preventing cancer progression.
In
addition, the researchers showed that only one concentration of retinoic acid
(about one micro Molar) produced the anti-cancer effects. Lower concentrations
gave no change, and higher concentrations produced a smaller effect.
The
next step will be to try to learn whether the amount of retinoic acid required
can be maintained in an animal model, and if that concentration will have the
same effects as Fernandez observed in cells.
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