# Synergistic Anticancer Effects of Apatinib and PD-L1 Inhibition in Breast Cancer

**Authors:** Danyang Han, Juanjuan Xu, Cairu Guo

PMC · DOI: 10.1007/s10911-026-09600-3 · Journal of Mammary Gland Biology and Neoplasia · 2026-01-31

## TL;DR

This study shows that combining apatinib and PD-L1 inhibitors can effectively fight breast cancer by reducing tumor growth and promoting cell death.

## Contribution

The study demonstrates a novel synergistic effect of apatinib and PD-L1 inhibition in breast cancer treatment.

## Key findings

- The combination significantly suppressed proliferation, migration, and invasion of breast cancer cells.
- The regimen promoted apoptosis and reduced levels of p-ERK, NF-κB, and Slug in vitro.
- The synergy was observed both in vitro and in vivo, suggesting clinical potential.

## Abstract

Studies in breast cancer have demonstrated that apatinib exhibits both antiangiogenic and antitumor effects, while PD-L1 inhibitors have similarly shown meaningful clinical benefit. Building upon these observations, this study evaluated the potential synergistic antitumor effects of combining apatinib with a PD-L1 inhibitor and examined the mechanistic basis for their interaction in breast cancer. Notably, we found that this regimen could significantly suppress the proliferation, migration, and invasion of MCF-7 and MDA-MB-231 cells, and promote cell apoptosis. In addition, the levels of p-ERK, NF-κB, and Slug were markedly reduced in vitro. Collectively, these findings support the potential clinical utility of combining apatinib and PD-L1 inhibition, as evidenced by consistent in vitro and in vivo synergy.

## Linked entities

- **Genes:** EPHB2 (EPH receptor B2) [NCBI Gene 2048], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], SNAI2 (snail family transcriptional repressor 2) [NCBI Gene 6591]
- **Chemicals:** apatinib (PubChem CID 45139106)
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, SNAI2 (snail family transcriptional repressor 2) [NCBI Gene 6591] {aka SLUG, SLUGH, SLUGH1, SNAIL2, WS2D}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}
- **Diseases:** Breast Cancer (MESH:D001943)
- **Chemicals:** Apatinib (MESH:C553458)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12948880/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12948880/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12948880/full.md

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Source: https://tomesphere.com/paper/PMC12948880