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May 27, 2026Molecules0 citationsOpen Access

Cypripedin Induces Apoptosis and Synergizes with Bortezomib via ER Stress Mediated Ubiquitination of GRP78 in T-Cell Acute Lymphoblastic Leukemia

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ZZZin ZinBNBodee NuthoBSBoonchoo Sritularak

Key Points

  • This study aims to evaluate the cytotoxic effects of cypripedin and its synergy with bortezomib in T-ALL cells.
  • Jurkat T-ALL cells were treated with 13 natural compounds at varying concentrations for 48 hours.
  • Cell viability was assessed using WST-1 assays; apoptosis was analyzed through flow cytometry and staining techniques.
  • Synergistic effects with bortezomib were assessed using a fixed-ratio combination index approach.
  • Cypripedin exhibited potent cytotoxicity with an IC50 of 6.52 µM and increased apoptosis in a dose-dependent manner.
  • Combination treatment reduced the bortezomib IC50 from 3.43 to 1.88 ng/mL, with a combination index (CI) of less than 0.5 indicating synergy.
  • Cypripedin activated ER stress markers and promoted GRP78 ubiquitination, supporting its pharmacological mechanism.

Abstract

Background: T-cell acute lymphoblastic leukemia (T-ALL) remains a challenging malignancy with limited targeted therapies. Natural phenanthrene derivatives represent a promising source of antileukemic agents. Objective: We screened a library of natural phenanthrene-type compounds to identify cytotoxic leads in Jurkat T-ALL cells and investigated the mechanisms underlying their activity, including potential synergy with the proteasome inhibitor bortezomib (BTZ). Methods: Jurkat cells were treated with thirteen natural compounds at 10 and 20 µM for 48 h; cell viability was assessed by WST-1 cell viability assay. Dose–response curves were generated to calculate IC50 values. Apoptosis was evaluated by Hoechst 33342/PI staining and Annexin V/PI flow cytometry. Synergy with BTZ was analyzed using a fixed-ratio combination index (CI) approach and IC50 shift analysis. ER stress signaling was characterized by Western blotting, quantitative RT-PCR of UPR genes (GRP78, ATF6), and immunoprecipitation of GRP78 followed by ubiquitin immunoblotting. Results: Among the compounds screened, Cypripedin showed the most potent cytotoxicity with an IC50 of 6.52 µM. It induced a dose-dependent increase in apoptosis. Combination with BTZ yielded a CI < 0.5 and reduced BTZ IC50 from 3.43 to 1.88 ng/mL. Cypripedin activated the unfolded protein response (UPR), modulated key ER stress markers including GRP78, p-PERK, p-eIF2α, p-JNK, and ATF6, downregulated UPR gene transcripts, and promoted GRP78 ubiquitination. Molecular docking predicted strong binding of Cypripedin to the GRP78 ATPase domain (Vina score −7.630 kcal/mol), supporting its mechanism of action. Conclusion: Cypripedin induces apoptosis in Jurkat T-ALL cells, synergizes with BTZ, and modulates ER stress through GRP78 ubiquitination. These findings support its further development as a potential T-ALL therapeutic.

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Cite This Study

Zin et al. (2026) studied this question.

synapsesocial.com/papers/6a168b040c924ddd1bd59d0chttps://doi.org/10.3390/molecules31111823
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