# Lead Decreases Bone Morphogenetic Protein-7 (BMP-7) Expression and Increases Renal Cell Carcinoma Growth in a Sex-Divergent Manner

**Authors:** Elizabeth A. Grunz, Haley Anderson, Rebecka M. Ernst, Spencer Price, D’Artanyan Good, Victoria Vieira-Potter, Alan R. Parrish

PMC · DOI: 10.3390/ijms25116139 · International Journal of Molecular Sciences · 2024-06-02

## TL;DR

This study shows that lead exposure increases kidney cancer growth in males but not females, possibly by reducing a protein called BMP-7.

## Contribution

The study reveals a sex-specific mechanism linking lead exposure to increased renal cell carcinoma progression via altered BMP-7 and sex hormone receptor expression.

## Key findings

- Lead exposure increases tumor size in male but not female mice.
- Lead reduces BMP-7 expression in tumors from male mice.
- Lead exposure alters androgen receptor expression in male tumor cells.

## Abstract

Both tissue and blood lead levels are elevated in renal cell carcinoma (RCC) patients. These studies assessed the impact of the subchronic lead challenge on the progression of RCC in vitro and in vivo. Lead challenge of Renca cells with 0.5 μM lead acetate for 10 consecutive passages decreased E-cadherin expression and cell aggregation. Proliferation, colony formation, and wound healing were increased. When lead-challenged cells were injected into mice, tumor size at day 21 was increased; interestingly, this increase was seen in male but not female mice. When mice were challenged with 32 ppm lead in drinking water for 20 weeks prior to tumor cell injection, there was an increase in tumor size in male, but not female, mice at day 21. To investigate the mechanism underlying the sex differences, the expression of sex hormone receptors in Renca cells was examined. Control Renca cells expressed estrogen receptor (ER) alpha but not ER beta or androgen receptor (AR), as assessed by qPCR, and the expression of ERα was increased in tumors in both sexes. In tumor samples harvested from lead-challenged cells, both ERα and AR were detected by qPCR, yet there was a significant decrease in AR seen in lead-challenged tumor cells from male mice only. This was paralleled by a plate-based array demonstrating the same sex difference in BMP-7 gene expression, which was also significantly decreased in tumors harvested from male but not female mice; this finding was validated by immunohistochemistry. A similar expression pattern was seen in tumors harvested from the mice challenged with lead in the drinking water. These data suggest that lead promotes RCC progression in a sex-dependent via a mechanism that may involve sex-divergent changes in BMP-7 expression.

## Linked entities

- **Genes:** BMP7 (bone morphogenetic protein 7) [NCBI Gene 655], shg (shotgun) [NCBI Gene 37386], Esr1 (estrogen receptor 1 (alpha)) [NCBI Gene 13982], ESR2 (estrogen receptor 2) [NCBI Gene 2100]
- **Proteins:** BMP7 (bone morphogenetic protein 7), shg (shotgun)
- **Chemicals:** lead (PubChem CID 5352425)
- **Diseases:** renal cell carcinoma (MONDO:0005086), RCC (MONDO:0005086)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Esr1 (estrogen receptor 1 (alpha)) [NCBI Gene 13982] {aka ER, ER-alpha, ERa, ERalpha, ESR, Estr}, Bmp7 (bone morphogenetic protein 7) [NCBI Gene 12162] {aka OP1}, Cdh1 (cadherin 1) [NCBI Gene 12550] {aka ARC-1, E-cad, Ecad, L-CAM, UVO, Um}, Esr2 (estrogen receptor 2 (beta)) [NCBI Gene 13983] {aka ER[b], ERbeta, Estrb}, Ar (androgen receptor) [NCBI Gene 11835] {aka Tfm}
- **Diseases:** tumor (MESH:D009369), RCC (MESH:D002292)
- **Chemicals:** Lead (MESH:D007854), lead acetate (MESH:C008261)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** Renca — Mus musculus (Mouse), Mouse kidney carcinoma, Cancer cell line (CVCL_2174)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11172964/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11172964/full.md

## References

69 references — full list in the complete paper: https://tomesphere.com/paper/PMC11172964/full.md

---
Source: https://tomesphere.com/paper/PMC11172964