Literature DB >> 11960340

Plant stress hormones suppress the proliferation and induce apoptosis in human cancer cells.

O Fingrut1, E Flescher.   

Abstract

Cellular stressors induce various outcomes including inhibition of cell proliferation and cell death. Sodium salicylate (SA), a plant stress hormone, can suppress the proliferation or cause apoptosis in certain mammalian cancer cells. Plant stress hormones are activators of cellular responses, including cell death, to diverse stress situations in plants. Thus, we hypothesized that plant stress hormones share the ability to adversely affect cancer cells. We found that the plant stress hormone SA suppressed proliferation of lymphoblastic leukemia, prostate, breast and melanoma human cancer cells. Jasmonic acid (JA), a plant stress hormone belonging to the Jasmonate family, induced death in lymphoblastic leukemia cells and caused suppression of cell proliferation in the other human cancer cells mentioned above. Another member of the Jasmonate family, methyl jasmonate (MJ), induced death in each of the cell lines. Plant stress hormones did not affect normal human lymphocytes, in contrast to their strong effect on lymphoblastic leukemia cells. JA and MJ caused apoptotic death, as determined by characteristic nuclear morphology, flow cytometric DNA profile and elevation of caspase-3 activity. Finally, mice bearing EL-4 lymphoma and treated with MJ, survived for significantly (P = 0.00953) longer periods of time than untreated mice. These findings suggest that plant stress hormones may potentially be a novel class of anti-cancer drugs.

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Year:  2002        PMID: 11960340     DOI: 10.1038/sj.leu.2402419

Source DB:  PubMed          Journal:  Leukemia        ISSN: 0887-6924            Impact factor:   11.528


  36 in total

1.  Methyljasmonate displays in vitro and in vivo activity against multiple myeloma cells.

Authors:  Steffen Klippel; Jana Jakubikova; Jake Delmore; Melissa Ooi; Douglas McMillin; Efstathios Kastritis; Jacob Laubach; Paul G Richardson; Kenneth C Anderson; Constantine S Mitsiades
Journal:  Br J Haematol       Date:  2012-09-13       Impact factor: 6.998

Review 2.  Production of cross-kingdom oxylipins by pathogenic fungi: An update on their role in development and pathogenicity.

Authors:  Gregory J Fischer; Nancy P Keller
Journal:  J Microbiol       Date:  2016-02-27       Impact factor: 3.422

Review 3.  Lipid analogues as potential drugs for the regulation of mitochondrial cell death.

Authors:  Michael Murray; Herryawan Ryadi Eziwar Dyari; Sarah E Allison; Tristan Rawling
Journal:  Br J Pharmacol       Date:  2014-04       Impact factor: 8.739

4.  Stress-responsive JNK mitogen-activated protein kinase mediates aspirin-induced suppression of B16 melanoma cellular proliferation.

Authors:  Orly Ordan; Ronit Rotem; Ilona Jaspers; Eliezer Flescher
Journal:  Br J Pharmacol       Date:  2003-03       Impact factor: 8.739

5.  Methyl jasmonate down-regulates survivin expression and sensitizes colon carcinoma cells towards TRAIL-induced cytotoxicity.

Authors:  Z Raviv; A Zilberberg; S Cohen; D Reischer-Pelech; C Horrix; M R Berger; R Rosin-Arbesfeld; E Flescher
Journal:  Br J Pharmacol       Date:  2011-11       Impact factor: 8.739

6.  Jasmonates induce nonapoptotic death in high-resistance mutant p53-expressing B-lymphoma cells.

Authors:  Orit Fingrut; Dorit Reischer; Ronit Rotem; Natalia Goldin; Irit Altboum; Israel Zan-Bar; Eliezer Flescher
Journal:  Br J Pharmacol       Date:  2005-11       Impact factor: 8.739

Review 7.  Mitochondrial metabolism inhibitors for cancer therapy.

Authors:  Emma E Ramsay; Philip J Hogg; Pierre J Dilda
Journal:  Pharm Res       Date:  2011-09-15       Impact factor: 4.200

8.  Targeting anthracycline-resistant tumor cells with synthetic aloe-emodin glycosides.

Authors:  Elinor Breiner-Goldstein; Zoharia Evron; Michael Frenkel; Keren Cohen; Keren Nir Meiron; Dan Peer; Yael Roichman; Eliezer Flescher; Micha Fridman
Journal:  ACS Med Chem Lett       Date:  2011-05-12       Impact factor: 4.345

9.  PI3K/Akt pathway activation attenuates the cytotoxic effect of methyl jasmonate toward sarcoma cells.

Authors:  Uri Elia; Eliezer Flescher
Journal:  Neoplasia       Date:  2008-11       Impact factor: 5.715

10.  Potential antimalarial activity of Methyl Jasmonate and its effect on lipid profiles in Plasmodium Berghei infected mice.

Authors:  Oladapo E Oyinloye; Ayokulehin M Kosoko; Benjamin Emikpe; Catherine O Falade; Olusegun G Ademowo
Journal:  Afr Health Sci       Date:  2015-09       Impact factor: 0.927

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