# Cytotoxicity of Cannabinoids in Combination with Traditional Lymphoma Chemotherapeutic Drugs Against Non-Hodgkin’s Lymphoma

**Authors:** Saba Omer, Mahmoud Mansour, Satyanarayana R Pondugula, Muralikrishnan Dhanasekaran, Brad Matz, Omer Khan, Dawn Boothe

PMC · DOI: 10.3390/biomedicines14010003 · Biomedicines · 2025-12-19

## TL;DR

This study shows that combining cannabinoids with traditional lymphoma drugs increases their effectiveness, potentially reducing drug toxicity and improving cancer treatment.

## Contribution

The study demonstrates synergistic cytotoxic effects of cannabinoids with NHL chemotherapy drugs at sub-IC50 concentrations.

## Key findings

- All three cannabinoids synergistically enhanced the cytotoxicity of traditional NHL chemotherapy drugs.
- Combination therapy may reduce drug doses and toxicity while improving survival in lymphoma.
- The Chou–Talalay method confirmed synergistic interactions with combination indices below 1.

## Abstract

Background: Cannabinoids (CBs) are FDA-approved for mitigating chemotherapy-induced side effects such as pain, nausea, and loss of appetite. Beyond palliative care, CBs exhibit anti-tumor properties in various cancers, including non-Hodgkin’s lymphoma (NHL). Previously, we demonstrated the cytotoxic effect of endogenous and exogenous cannabinoids on human and canine B- and T-cell-type NHL cell lines. The purpose of this study was to establish the cytotoxic effect of cannabinoids in combination with the components of CHOP and lomustine. This traditional NHL chemotherapy regimen comprises cyclophosphamide, doxorubicin, vincristine, and prednisolone. Methods: In this study, we studied three cannabinoids, one from each of the three major categories of cannabinoids (endocannabinoid AEA, phytocannabinoid CBD, and synthetic cannabinoid WIN-55 212 22). Each cannabinoid was selected based on potency, as determined in our previous experiments. For the combination, we used five NHL chemotherapy drugs. We analyzed the cytotoxicity of each drug alone and in combinations using canine malignant B-type NHL cell line 1771 and a colorimetric MTT (3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyl tetrazolium bromide) cell proliferation assay and combination index (CI) based on the Chou–Talalay method. Results: Our results demonstrate that the cytotoxic effects of all traditional NHL chemotherapy drugs are synergistically enhanced (interaction with CI < 1) by each of the three cannabinoids at sub-IC50 concentrations. Conclusions: This work provides a proof of concept for using cannabinoids and traditional NHL drugs in combination to reduce the dose, and thereby potentially reducing the toxicity, of chemotherapeutic drugs and increasing the survival benefit in lymphoma clinical translation studies, offering a significant advancement in cancer treatment.

## Linked entities

- **Chemicals:** cannabinoids (PubChem CID 9852188), cyclophosphamide (PubChem CID 2907), doxorubicin (PubChem CID 31703), vincristine (PubChem CID 5978), prednisolone (PubChem CID 5755), lomustine (PubChem CID 3950), AEA (PubChem CID 5281969), CBD (PubChem CID 644019)
- **Diseases:** non-Hodgkin’s lymphoma (MONDO:0018908), NHL (MONDO:0018908)

## Full-text entities

- **Diseases:** loss of appetite (MESH:D001068), Lymphoma (MESH:D008223), Cytotoxicity (MESH:D064420), cancer (MESH:D009369), B- and T-cell-type NHL (MESH:D016393), NHL (MESH:D008228), nausea (MESH:D009325), pain (MESH:D010146)
- **Chemicals:** endocannabinoid (MESH:D063388), AEA (-), lomustine (MESH:D008130), CBs (MESH:D002186), 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyl tetrazolium bromide (MESH:C022616), MTT (MESH:C070243)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12837863/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12837863/full.md

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Source: https://tomesphere.com/paper/PMC12837863