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Influence of vitamin D signaling on hormone receptor status and HER2 expression in breast cancer

  • Review – Cancer Research
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Journal of Cancer Research and Clinical Oncology Aims and scope Submit manuscript

Abstract

Purpose

Breast cancer is a significant global public health issue. It is the leading cause of death among women around the world, with an incidence increasing annually. In recent years, there has been more and more information in the literature regarding a protective role of vitamin D in cancer. Increasingly preclinical and clinical studies suggest that vitamin D optimal levels can reduce the risk of breast cancer development and regulate cancer-related pathways.

Method

In this review, we focus on the importance of vitamin D in breast cancers, discussing especially the influence of vitamin D signaling on estrogen receptor and human epidermal growth factor receptor 2 (HER2), two major biomarkers of breast cancer today.

Conclusion

We discuss the possibility of actual and future targeted therapeutic approaches for vitamin D signaling in breast cancer.

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Abbreviations

AIs:

Aromatase inhibitors

ARs:

Retinoic acid receptors

BC:

Breast cancer

cAMP:

Cyclic adenosine monophosphate

CRE:

cAMP-responsive element

CDH1:

Cadherin 1

CDK:

Cyclin-dependent kinase

COX2:

Cyclooxygenase 2

CTSL:

Cathepsin L

CYP:

Cytochrome P450

CYP27A1:

25α-Hydroxylase

CYP27B1:

1α-Hydroxylase

DBD:

DNA-binding domain

DFS:

Disease-free survival

EDF:

Endoxifen

ER:

Estrogen receptor

FXRs:

Farnesoid X receptors

HER2:

Human epidermal growth factor receptor 2

HIF1α:

Hypoxia-inducible factor 1α

HDT:

4-Hydroxytamoxifen

IGF:

Insulin-like growth factor

IGF1:

Insulin-like growth factor 1

IL-6:

Interleukin-6

LBD:

Ligand-binding domain

LXRs:

Liver X receptors

MAPKP5:

Mitogen-activated protein kinase phosphatase 5

MMP1:

Matrix metalloproteinase 1

MMP9:

Matrix metalloproteinase 9

NDT:

N-desmethyl tamoxifen

NF-κB:

Nuclear factor-κB

NRs:

Nuclear hormone receptors

OS:

Overall survival

PPARs:

Peroxisome proliferator-activated receptors

PARPi:

Inhibitors of poly(ADP-ribose) polymerase

PG:

Prostaglandin

15-PGDH:

15-Hydroxyprostaglandin dehydrogenase

PGE2:

Prostaglandin E2

PR:

Progesterone receptor

RTKs:

Receptor tyrosine kinases

RXRs:

Retinoid X receptors

SAM:

Selective aromatase modulators

STAT3:

Signal transducer and activator of transcription 3

TGF-β:

Transforming growth factor-β

TNF-α:

Tumor necrosis factor-α

SERMs:

Selective ER modulators

SERDs:

Selective ER down-regulators

SNPs:

Germline single nucleotide polymorphisms

TAM:

Tamoxifen

TIMP1:

Tissue inhibitor of metalloproteinases 1

TNBC:

Triple-negative breast cancers

TRs:

Thyroid hormone receptors

VDR:

Vitamin D receptor

VDREs:

Vitamin D response elements

VEGF:

Vascular endothelial growth factor

References

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Funding

XZ was supported by the China Scholarship Council (CSC) with a 2-year stipend (File No 201508080093). SDS salary was supported by the University Paul Sabatier in Toulouse (France).

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Authors

Corresponding author

Correspondence to Sophie Doisneau-Sixou.

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Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

This article does not contain any studies with human participants or animals performed by any of the authors.

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Zhang, X., Harbeck, N., Jeschke, U. et al. Influence of vitamin D signaling on hormone receptor status and HER2 expression in breast cancer. J Cancer Res Clin Oncol 143, 1107–1122 (2017). https://doi.org/10.1007/s00432-016-2325-y

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  • DOI: https://doi.org/10.1007/s00432-016-2325-y

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