AI Article Synopsis

  • The hexane fraction of Danshen, derived from the root of Salvia miltiorrhiza, demonstrates the ability to inhibit the growth of human leukemia cells through its active compounds.
  • One specific compound, trijuganone C (Compound 2), exhibited strong antiproliferative effects on various leukemia and colon cancer cell lines, with IC values below 10 μM.
  • The mechanism of action for Compound 2 involves inducing apoptosis through mitochondrial dysfunction and the activation of specific caspases, suggesting its potential as a chemotherapeutic agent for treating leukemia.

Article Abstract

In this study, we found that the hexane fraction of Danshen, the dried root of Salvia miltiorrhiza (Lamiaceae), exerted antiproliferative effects on human leukemia cells. Phytochemical investigation of the hexane fraction achieved the isolation of the tanshinone diterpenes: dihydrotanshinone I (1), trijuganone C (2), trijuganone B (3), cryptotanshinone (4), tanshinone IIA (5), and tanshinone I (6). Compound 2 showed significant antiproliferative activities against human leukemia cells HL-60, Jurkat, and U937. The antiproliferative activities of 2 against human cancer and normal cells indicated that 2 exhibited potent antiproliferative activities with IC values less than 10 μM against HL-60 and Jurkat cells as well as on the colon cancer cells DLD-1, COLO 205, and Caco-2. Compound 2 induced chromatin condensation, DNA fragmentation, activation of caspase-3, -8, and -9, and the cleavage of poly (ADP-ribose) polymerase (PARP) in HL-60 cells. Moreover, 2 activated Bid and Bax, leading to the loss of mitochondrial membrane potential, and 2 induced the cytochrome c release from mitochondria into cytosol. In contrast, Bcl-2 and Bcl-xL were unaffected by 2. These results suggest that 2 exerts antiproliferative effects via apoptosis induction mediated by mitochondrial dysfunction and caspase activation. Compound 2 may serve as a candidate of potential chemotherapeutic agent for human leukemia.

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Source
http://dx.doi.org/10.1002/ptr.6013DOI Listing

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