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Houttuynia cordata Thunb. Essential Oil Inhibits Diffuse Large B-cell lymphoma Growth
Youmei Peng1, Shangkun Liu1,2, Xiaoqian Fu1,2
1Henan Key Laboratory for Pharmacology of liver diseases, BGI College & Henan Institute of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, CHINA.
Journal of Oleo Science
|March 1, 2026
Summary
Houttuynia cordata Thunb. Essential Oil (HEO) shows anti-tumor effects against Diffuse Large B-cell Lymphoma (DLBCL). HEO inhibits DLBCL cell proliferation and tumor growth by suppressing the PI3K/Akt signaling pathway.
Area of Science:
- Oncology
- Pharmacology
- Natural Products
Background:
- Diffuse Large B-cell Lymphoma (DLBCL) is a prevalent non-Hodgkin lymphoma subtype with poor prognosis and limited effective treatments.
- Houttuynia cordata Thunb. is an Asian medicinal plant with known anti-inflammatory and anti-tumor properties.
Purpose of the Study:
- To investigate the therapeutic potential of Houttuynia cordata Thunb. Essential Oil (HEO) in Diffuse Large B-cell Lymphoma (DLBCL).
- To elucidate the underlying molecular mechanisms of HEO's anti-tumor activity in DLBCL.
Main Methods:
- In vitro studies on DLBCL cell lines (SUDHL-4) to assess proliferation, apoptosis, and cell cycle.
- In vivo studies using a DLBCL athymic nude mouse xenograft model to evaluate tumor growth inhibition.
- Network pharmacology analysis and phospho-specific protein microarray to identify regulated signaling pathways.
- Western blot analysis to confirm protein expression changes and compound-target docking to identify active components.
Main Results:
- HEO inhibited DLBCL cell proliferation and induced apoptosis and G0/G1 cell cycle arrest in a dose-dependent manner.
- HEO significantly suppressed DLBCL tumor growth in vivo with no observed toxicity.
- HEO was found to downregulate the PI3K/Akt signaling pathway, reducing p-PI3K and p-Akt levels.
- HEO modulated apoptosis-related proteins, decreasing Bcl-2 and increasing Bax and caspase-3 expression.
- Key HEO components like bornyl acetate, caryophyllene oxide, and terpineol showed strong binding affinity to PI3K and Akt.
Conclusions:
- HEO exhibits significant anti-tumor effects against DLBCL through the inhibition of the PI3K/Akt signaling pathway.
- HEO demonstrates potential as a novel therapeutic agent for DLBCL treatment by targeting the PI3K/Akt pathway.
- The identified active components of HEO contribute to its therapeutic efficacy in DLBCL.
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