Title | Induction of murine embryonic stem cell differentiation by medicinal plant extracts. |
Publication Type | Journal Article |
Year of Publication | 2011 |
Authors | Reynertson KA, Charlson ME, Gudas LJ |
Journal | Exp Cell Res |
Volume | 317 |
Issue | 1 |
Pagination | 82-93 |
Date Published | 2011 Jan 01 |
ISSN | 1090-2422 |
Keywords | Alkaline Phosphatase, Animals, Cell Differentiation, Cell Proliferation, Cells, Cultured, Dose-Response Relationship, Drug, Embryonic Stem Cells, Gene Expression Regulation, Developmental, Humans, Mice, Plant Extracts, Plants, Medicinal, Quassia, Simarouba, Up-Regulation |
Abstract | Epidemiological evidence indicates that diets high in fruits and vegetables provide a measure of cancer chemoprevention due to phytochemical constituents. Natural products are a rich source of cancer chemotherapy drugs, and primarily target rapidly cycling tumor cells. Increasing evidence indicates that many cancers contain small populations of resistant, stem-like cells that have the capacity to regenerate tumors following chemotherapy and radiation, and have been linked to the initiation of metastases. Our goal is to discover natural product-based clinical or dietary interventions that selectively target cancer stem cells, inducing differentiation. We adapted an alkaline phosphatase (AP) stain to assay plant extracts for the capacity to induce differentiation in embryonic stem (ES) cells. AP is a characteristic marker of undifferentiated ES cells, and this represents a novel approach to screening medicinal plant extracts. Following a survey of approximately 100 fractions obtained from 12 species of ethnomedically utilized plants, we found fractions from 3 species that induced differentiation, decreasing AP and transcript levels of pluripotency markers (Nanog, Oct-4, Rex-1). These fractions affected proliferation of murine ES, and human embryonal, prostate, and breast carcinoma cells in a dose-dependent manner. Several phytochemical constituents were isolated; the antioxidant phytochemicals ellagic acid and gallic acid were shown to affect viability of cultured breast carcinoma cells. |
DOI | 10.1016/j.yexcr.2010.10.010 |
Alternate Journal | Exp. Cell Res. |
PubMed ID | 20955699 |
PubMed Central ID | PMC3179386 |
Grant List | T32 AT001161 / AT / NCCIH NIH HHS / United States T32 AT001161-01A1 / AT / NCCIH NIH HHS / United States T32AT001161 / AT / NCCIH NIH HHS / United States |