# Temozolomide increases the generation of cell heterogeneity in ERK activity in glioma cells

**Authors:** Karine Rech Begnini, Julia Caroline Marcolin, Luiza Cherobini Pereira, Letícia Cunha Pereira de Souza, Frederico Kraemer-Mattos, Daphne Tórgo, Carolina Machemer, Georgia da Silva Goulart, Andrew Oliveira Silva, Jephesson Alex Floriano dos Santos, Guido Lenz

PMC · DOI: 10.1007/s00109-026-02644-2 · 2026-01-29

## TL;DR

This study shows that the chemotherapy drug temozolomide increases ERK activity variability in glioblastoma cells, which affects their survival and response to treatment.

## Contribution

The study reveals that temozolomide induces ERK heterogeneity in clonal glioblastoma populations, impacting therapy outcomes.

## Key findings

- ERK activity in glioblastoma cells is highly variable under normal conditions.
- Temozolomide increases ERK heterogeneity even in clonal cell populations.
- Reducing ERK heterogeneity with trametinib improves treatment effectiveness.

## Abstract

ERK activity governs diverse cellular responses and has significant implications in cancer biology and treatment. Cellular heterogeneity is a major feature of cancer and a barrier for therapy success, allowing cancer cells to adapt and survive in challenging environments. Here, we used a genetic live-cell reporter to explore the heterogeneity of ERK signaling activity within cellular populations and colonies of glioblastoma (GB) cells. GB cells showed a wide spectrum of ERK activation levels in basal culture conditions and throughout state transitions. Treatment with the chemotherapeutic agent temozolomide increased the phenotypic heterogeneity in ERK activity within cells even in clonal populations. Using the MEK inhibitor trametinib in combination with temozolomide to homogenize ERK activity reduced cell fitness in colonies and decreased fractional killing in GB clonal cells. Our study contributes to the growing understanding of the complexity in ERK activity and dynamics, pointing out the consequences of cell-to-cell ERK phenotypic variability in fitness and therapy survival. The complexity of ERK signaling phenotypes in the context of chemotherapy treatment is shown, offering valuable insights about the intricacies of ERK signaling heterogeneity and chemotherapy treatment.

Heterogeneity in ERK activity in live GBM cells is high in basal culture conditions.Temozolomide alters ERK activity in GBM cells and generates phenotypic heterogeneity.Clonal populations behave heterogeneously in ERK activity, and this heterogeneity impacts fitness.Targeting the generation of ERK heterogeneity reduces fitness and fractional killing in GBM colonies.

Heterogeneity in ERK activity in live GBM cells is high in basal culture conditions.

Temozolomide alters ERK activity in GBM cells and generates phenotypic heterogeneity.

Clonal populations behave heterogeneously in ERK activity, and this heterogeneity impacts fitness.

Targeting the generation of ERK heterogeneity reduces fitness and fractional killing in GBM colonies.

The online version contains supplementary material available at 10.1007/s00109-026-02644-2.

## Linked entities

- **Proteins:** EPHB2 (EPH receptor B2), MAP2K7 (mitogen-activated protein kinase kinase 7)
- **Chemicals:** temozolomide (PubChem CID 5394), trametinib (PubChem CID 11707110)
- **Diseases:** glioblastoma (MONDO:0018177)

## Full-text entities

- **Genes:** Mapk1 (mitogen-activated protein kinase 1) [NCBI Gene 26413] {aka 9030612K14Rik, ERK, Erk2, MAPK2, PRKM2, Prkm1}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882] {aka AFR1, RAF}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}, Bach1 (BTB and CNC homology 1, basic leucine zipper transcription factor 1) [NCBI Gene 12013] {aka 6230421P05Rik}, Jun (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 16476] {aka AP-1, Junc, c-jun}, TP53BP1 (tumor protein p53 binding protein 1) [NCBI Gene 7158] {aka 53BP1, TDRD30, p202, p53BP1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, Egfr (epidermal growth factor receptor) [NCBI Gene 13649] {aka 9030024J15Rik, Erbb, Errb1, Errp, Wa5, wa-2}
- **Diseases:** PD (MESH:D005671), GBM (MESH:D005910), GB (MESH:D005909), Tumor (MESH:D009369), melanoma (MESH:D008545), tumorigenesis (MESH:D063646)
- **Chemicals:** phenol red (MESH:D010637), polybrene (MESH:D006583), glucose (MESH:D005947), DMEM (-), L-glutamine (MESH:D005973), PD184352 (MESH:C120227), TRAM (MESH:C560077), penicillin (MESH:D010406), streptomycin (MESH:D013307), DMSO (MESH:D004121), TMZ (MESH:D000077204), CO2 (MESH:D002245)
- **Species:** Mycoplasma (genus) [taxon 2093], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** U138 — Homo sapiens (Human), Astrocytoma, Cancer cell line (CVCL_0020), HTB-16 — Mus musculus (Mouse), Hybridoma (CVCL_A8FQ), MRC5 — Homo sapiens (Human), Finite cell line (CVCL_0440), Hek-293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), CCL-171 — Mus musculus (Mouse), Undefined cell line type (CVCL_M023), A172 — Homo sapiens (Human), Glioblastoma, Cancer cell line (CVCL_0131), U-251 MG — Homo sapiens (Human), Astrocytoma, Cancer cell line (CVCL_0021), CRL-1573 — Sigmodon hispidus (Hispid cotton rat), Spontaneously immortalized cell line (CVCL_YD58)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12855392/full.md

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Source: https://tomesphere.com/paper/PMC12855392