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Introduction: What they say

Noble laureate in Physiology/Medicine (1975) Prof. David Baltimore, from California Institute of Technology, California, USA, had reported in the July 8, 2014 issue of the Journal “Blood” that: “Dual mechanisms by which MiR-125b represses IRF4 to induce myeloid/B-cell leukemias.” 


What we say:

On the foundation of this interesting finding, Dr L Boominathan PhD, Director-cum-chief Scientist of GBMD, reports that: Natural product-derived therapy for Human Leukemias: Parthenolide, one of the main components of feverfew, suppresses B-Cell and myeloid leukemias via up regulation of the tumor suppressor IRF4


From Research findings to Therapeutic opportunity:

This study suggests that Parthenolide, by increasing the expression of  its target gene, it may increase the expression of a number of tumor suppressor genes, including IRF4. Thereby, it could inhibit the progression of B-Cell and myeloid leukemias (fig. 1).

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Taken together, this study suggests that pharmacological formulations encompassing       “Parthenolide or its analogues or Parthenolide in combination with other anticancer drugs may be used to inhibit B-Cell and myeloid leukemias.

parthenolide-induces-the-expression-of-irf4

Figure 1 Mechanistic insight into how Parthenolide increases the expression of IRF4 to prevent cancer progression


Details of the research details

Idea Proposed/Formulated byDr L Boominathan Ph.D.

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Undisclosed mechanistic information: How Parthenolide increases the expression of IRF4?

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References:

Web: http://genomediscovery.org or newbioideas.com

CitationBoominathan, L., Natural product-derived therapy for Human Leukemias: Parthenolide, one of the main components of feverfew, suppresses B-Cell and myeloid leukemias via up regulation of the tumor suppressor IRF4, 5/January/2016, 10.27 pm,  Genome-2-Bio-Medicine Discovery Center.

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