# Cytotoxicity Potency of Cannabinoids Is by Serum Supplementation: Implications for In Vitro Cancer Studies

**Authors:** Sanele Priscillia Mathibela, Maphuti Tebogo Lebelo, Vanessa Steenkamp

PMC · DOI: 10.1002/cnr2.70520 · 2026-03-11

## TL;DR

This study shows that the effectiveness of cannabinoids in killing cancer cells in lab tests depends on the amount of fetal calf serum in the culture medium.

## Contribution

The study reveals that low serum conditions enhance the cytotoxic effects of cannabinoids, offering a new insight into optimizing in vitro cancer research.

## Key findings

- CBD and THC showed significantly higher cytotoxicity in low-serum (0.5% FCS) conditions compared to standard (10% FCS) conditions.
- THC was more cytotoxic than CBD in SiHa cells, while both had similar effects in HeLa cells.
- Reduced serum concentration increases cannabinoid efficacy by limiting protein binding.

## Abstract

Fetal calf serum (FCS) is a key supplement in cell culture, providing nutrients, and growth factors that support cancer cell proliferation. Studies suggest that compound cytotoxicity profiles in vitro vary depending on FCS concentration in culture medium. The study aimed to examine how extracellular conditions influence the in vitro response of cancer cells to phytocannabinoids, with particular emphasis on serum supplementation.

Cells were exposed to CBD and THC in media containing 0.5% or 10% FCS for 24–72 h. Cell viability was assessed using the sulforhodamine B assay and live‐cell imaging. Significantly enhanced cytotoxic effects of CBD and THC were noted under low‐serum conditions (0.5% FCS) compared to standard conditions (10% FCS), particularly after 72 h incubation. THC demonstrated greater cytotoxicity than CBD in SiHa cells, while both compounds showed similar effects in HeLa cells.

The study demonstrates that serum concentration critically modulates the cytotoxic potency of cannabinoids. Reduced FCS enhances cannabinoid efficacy by limiting protein binding, emphasizing the need to optimize serum conditions for accurate in vitro cytotoxicity assessments.

## Linked entities

- **Chemicals:** CBD (PubChem CID 644019), THC (PubChem CID 16078)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** SPARC (secreted protein acidic and cysteine rich) [NCBI Gene 6678] {aka BM-40, OI17, ON, ONT}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, CNR2 (cannabinoid receptor 2) [NCBI Gene 1269] {aka CB-2, CB2, CX5}, TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, CNR1 (cannabinoid receptor 1) [NCBI Gene 1268] {aka CANN6, CB-R, CB1, CB1A, CB1K5, CB1R}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** cancer (MESH:D009369), pain (MESH:D010146), Cervical cancer (MESH:D002583), inflammatory (MESH:D007249), chronic pain (MESH:D059350), Cytotoxicity (MESH:D064420), epilepsy (MESH:D004827)
- **Chemicals:** acetic acid (MESH:D019342), Anandamide (MESH:C078814), water (MESH:D014867), 5-fluorouracil (MESH:D005472), streptomycin (MESH:D013307), versene (MESH:D004492), hydrocortisone (MESH:D006854), THC (MESH:D013759), Fluorescein diacetate (MESH:C018506), PI (MESH:D010716), methanol (MESH:D000432), trypan blue (MESH:D014343), platinum (MESH:D010984), capsazepine (MESH:C071423), Cannabinoids (MESH:D002186), calcium (MESH:D002118), CBD (MESH:D002185), DMSO (MESH:D004121), endocannabinoid (MESH:D063388), CO2 (MESH:D002245), l-glutamine (MESH:D005973), SRB (MESH:C022027), VC (MESH:C098534), TCA (MESH:D014238), amino acids (MESH:D000596), fungizone (MESH:D000666), penicillin (MESH:D010406), CBD (-), propidium iodide (MESH:D011419), Cisplatin (MESH:D002945)
- **Species:** Cannabis (genus) [taxon 3482], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C-45 C
- **Cell lines:** HTB-35 — Mus musculus (Mouse), Hybridoma (CVCL_A8FQ), SiHa — Homo sapiens (Human), Human papillomavirus-related cervical squamous cell carcinoma, Cancer cell line (CVCL_0032), CCL-2 — Mus musculus (Mouse), Undefined cell line type (CVCL_M023), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320), MCF-12A — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_3744), Caski — Homo sapiens (Human), Human papillomavirus-related cervical squamous cell carcinoma, Cancer cell line (CVCL_1100), CRL-10782 — Homo sapiens (Human), Amyotrophic lateral sclerosis, Transformed cell line (CVCL_BF13)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12977297/full.md

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Source: https://tomesphere.com/paper/PMC12977297