Photo Credit - Tony Hisgett via WikiMedia Creative Commons |
The
paper from #BethIsraelDeaconessMedicalCenter and the #CancerResearchInstitute shows cancer can be effectively targeted with i3C,
a molecule found in broccoli and other cruciferous vegetables.
The findings state that because ‘an increased expression level of… PTEN impairment is widely pervasive in various human cancers, targeting this pathway toward PTEN reactivation may represent an “Achilles heel” of broad application.’
The i3C broccoli molecule
had both tumour-preventative and tumour-suppressive effects.
i3C (indole-3-carbinol)
was found to rebalance and reactivate an important gene for tumour suppression
called PTEN. (PTEN is a gene that in ideal genetic conditions, controls and
prevents the growth of cancer.)
The group’s experiments
established WWP1 produces an enzyme that causes PTEN to malfunction. It can be over-
or underactive, but in both cases i3C aided in restoring normal activity and resulted
in tumour cell suppression and abatement (in mice and in human tissue samples).
In hereditary
predispositions to cancer, PTEN is likely to have been mutated and it is also
one of the more vulnerable genes to changes that predicate malignancies.
Last month’s revelation
has also re-energized academic discourse around the subject of broccoli and cancer
prevention, indicated by a sharp increase in i3C studies released and even re-released.
Broccoli’s anti-cancer benefits are well known, and in part this common awareness was said to have prompted
the research institute’s inclusion of i3C in the WWP1 study.
A study of i3C effects
on liver cancer was published
last year with researchers suggesting positive indicators of its dual potential
as a preventative and treatment.
The Beth Israel
research group (which is affiliated with Harvard University Medical School) are keen to further explore possibilities of i3C, and CRISPR
technology, for PTEN restoration.
They plan to study WWP1 and more potent
inhibitors, and they asserted that these findings “pave the way” towards development
of a tumour-suppressor reactivation approach to cancer treatment.###