An Ingenane-Type Diterpene from Promoted Cell Apoptosis and Macrophage Polarization via the Regulation of PKC Signaling Pathways.

Int J Mol Sci

Center for Pharmaceutical Sciences and Engineering, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.

Published: September 2024

AI Article Synopsis

  • The text discusses a toxic Chinese medicine known for its long history of use, which is believed to help with water retention and swelling.
  • The main active compounds in this medicine are diterpenes and triterpenes, specifically ingenane-type diterpenes, which have been shown to have anti-cancer properties by activating a protein called PKC-δ.
  • A specific compound, known as compound A, was found to inhibit cancer cell proliferation and influence how macrophages function, showing potential for new cancer treatments through immune cell regulation.

Article Abstract

, a toxic Chinese medicine used for more than 2000 years, has the effect of "purging water to promote drinking" and "reducing swelling and dispersing modules". Diterpenes and triterpenes are the main bioactive components of . Among them, ingenane-type diterpenes have multiple biological activities as a protein kinase C δ (PKC-δ) activator, which have previously been shown to promote anti-proliferative and pro-apoptotic effects in several human cancer cell lines. However, the activation of PKC subsequently promoted the survival of macrophages. Recently, we found that 13-hydroxyingenol-3-(2,3-dimethylbutanoate)-13-dodecanoate (compound A) from showed dual bioactivity, including the inhibition of tumor-cell-line proliferation and regulation of macrophage polarization. This study identifies the possible mechanism of compound A in regulating the polarization state of macrophages, by regulating PKC-δ-extracellular signal regulated kinases (ERK) signaling pathways to exert anti-tumor immunity effects in vitro, which might provide a new treatment method from the perspective of immune cell regulation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11432454PMC
http://dx.doi.org/10.3390/ijms251810123DOI Listing

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