# Novel Small Molecule DZ-865B Effectively Degrades BCL6, Promotes Apoptosis and Reduces Proliferation of Diffuse Large B-Cell Lymphoma Cells

**Authors:** Yanfeng Wang, Xinyi Chen, Yichen Yin, Tao Li, Jing Chen

PMC · DOI: 10.32604/or.2026.068695 · Oncology Research · 2026-02-24

## TL;DR

A new small molecule called DZ-865B degrades BCL6 protein in lymphoma cells, causing cell death and reduced growth, offering a potential treatment for diffuse large B-cell lymphoma.

## Contribution

DZ-865B is a novel PROTAC-based molecule that effectively degrades BCL6 and inhibits DLBCL progression.

## Key findings

- DZ-865B degrades BCL6 in DLBCL cells via the ubiquitin-proteasome pathway.
- DZ-865B induces apoptosis and inhibits DNA synthesis in DLBCL cell lines.
- BCL6 overexpression is confirmed in DLBCL using TCGA and experimental validation.

## Abstract

B-cell lymphoma 6 (BCL6) is a transcriptional repressor whose overexpression is closely linked to the progression of diffuse large B-cell lymphoma (DLBCL), making it a promising therapeutic target. This study aims to identify a novel small molecule, synthesized via proteolysis-targeting chimeras (PROTACs), capable of degrading BCL6, thereby inhibiting DLBCL growth and providing a foundation for future preclinical studies.

The expression of BCL6 in DLBCL was analyzed using The Cancer Genome Atlas (TCGA) database and the Human Protein Atlas. Western blotting assays confirmed BCL6 expression in tumor cell lines, leading to the identification of the small molecule compound DZ-865B. To evaluate DZ-865B’s in vitro efficacy, multiple assays were performed, including protein immunoblotting, immunofluorescence, reverse transcription quantitative PCR, EDU proliferation, and soft agar cloning assays.

TCGA analysis revealed significant overexpression of BCL6 in DLBCL (p < 0.05), corroborated by immunohistological staining and western blotting. DZ-865B induced BCL6 degradation in DLBCL cell lines (OCI-LY-1 and SU-DHL-4) in a concentration- and time-dependent manner, and induced the degradation of nuclear BCL6 through the ubiquitin-proteasome pathway. Notably, DZ-865B did not alter BCL6 mRNA levels but modulated downstream gene expression, leading to the activation of apoptosis pathway proteins and inhibition of DNA synthesis, effectively suppressing DLBCL cell growth.

This study demonstrates that the small molecule DZ-865B targets and degrades BCL6 in DLBCL cells, promoting apoptosis and inhibiting cellular proliferation. These findings highlight DZ-865B as a potential therapeutic agent for diffuse large B-cell lymphoma.

## Linked entities

- **Genes:** BCL6 (BCL6 transcription repressor) [NCBI Gene 604]
- **Proteins:** BCL6 (BCL6 transcription repressor)
- **Diseases:** diffuse large B-cell lymphoma (MONDO:0018905), DLBCL (MONDO:0018905)

## Full-text entities

- **Genes:** MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, BCL6 (BCL6 transcription repressor) [NCBI Gene 604] {aka BCL5, BCL6A, LAZ3, ZBTB27, ZNF51}, BCL2L1 (BCL2 like 1) [NCBI Gene 598] {aka BCL-XL/S, BCL2L, BCLX, Bcl-X, PPP1R52}, CAT (catalase) [NCBI Gene 847], GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, CRBN (cereblon) [NCBI Gene 51185] {aka MRT2, MRT2A}, SIAH1 (siah E3 ubiquitin protein ligase 1) [NCBI Gene 6477] {aka BURHAS, SIAH1A}, MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, POTEF (POTE ankyrin domain family member F) [NCBI Gene 728378] {aka A26C1B, POTE2alpha, POTEACTIN}, CDKN1A (cyclin dependent kinase inhibitor 1A) [NCBI Gene 1026] {aka CAP20, CDKN1, CIP1, MDA-6, P21, SDI1}
- **Diseases:** follicular lymphoma (MESH:D008224), pocket cell lymphoma (MESH:D016399), leukemia (MESH:D007938), marginal zone lymphoma (MESH:D018442), cytotoxicity (MESH:D064420), Lymphoma (MESH:D008223), B-Cell Lymphoma (MESH:D016393), triple-negative breast cancer (MESH:D064726), breast cancer (MESH:D001943), NHL (MESH:D008228), ovarian cancer (MESH:D010051), DLBCL (MESH:D016403), inflammatory (MESH:D007249), glioma (MESH:D005910), CLL (MESH:D015451), Cancer (MESH:D009369), Gastric cancer (MESH:D013274), acute myeloid leukemia (MESH:D015470), paraneoplastic (MESH:D010257), NSCLC (MESH:D002289), GCB (MESH:D054331)
- **Chemicals:** BI-3802 (-), penicillin (MESH:D010406), Asp (MESH:D001224), Fluorescein (MESH:D019793), Hoechst 33342 (MESH:C017807), Ser (MESH:D012694), CO2 (MESH:D002245), Gln (MESH:D005973), Cys (MESH:D003545), paraformaldehyde (MESH:C003043), Lys (MESH:D008239), Trp (MESH:D014364), Hydrogen (MESH:D006859), formaldehyde (MESH:D005557), DMSO (MESH:D004121), DAPI (MESH:C007293), Thr (MESH:D013912), Met (MESH:D008715), FITC (MESH:D016650), His (MESH:D006639), sulfonamide (MESH:D013449), agar (MESH:D000362), Triton X-100 (MESH:D017830), streptomycin (MESH:D013307), Tyr (MESH:D014443), water (MESH:D014867), MG-132 (MESH:C072553), EdU (MESH:C022811), SDS (MESH:D012967)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Mycoplasma (genus) [taxon 2093]
- **Mutations:** Glu 237, Asp
- **Cell lines:** MDA-MB-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062), BT-549 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_1092), OCI-LY-1 — Homo sapiens (Human), Diffuse large B-cell lymphoma, Cancer cell line (CVCL_1879), HGC-27 — Homo sapiens (Human), Gastric carcinoma, Cancer cell line (CVCL_1279), NCI-H441 — Homo sapiens (Human), Lung papillary adenocarcinoma, Cancer cell line (CVCL_1561), BT-20 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0178), SU-DHL-4 — Homo sapiens (Human), Diffuse large B-cell lymphoma germinal center B-cell type, Cancer cell line (CVCL_0539), A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), MKN-45 — Homo sapiens (Human), Gastric adenocarcinoma, Cancer cell line (CVCL_0434), 60267-1 — Homo sapiens (Human), Cerebral palsy, Induced pluripotent stem cell (CVCL_LJ23), NCI-H1299 — Homo sapiens (Human), Lung large cell carcinoma, Cancer cell line (CVCL_0060), GES-1 — Homo sapiens (Human), Transformed cell line (CVCL_EQ22), BEAS-2B — Homo sapiens (Human), Transformed cell line (CVCL_0168), AGS — Homo sapiens (Human), Gastric adenocarcinoma, Cancer cell line (CVCL_0139)

## Full text

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## Figures

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963665/full.md

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Source: https://tomesphere.com/paper/PMC12963665