Breast cancer during pregnancy of Luminal A type overexpressed CXCL13

Author:

Nozaki Fumi1ORCID,Nakanishi Yoko1,Tanino Tomoyuki1,Ochi Tomohiro2,In Reika23,Kajiura Yuka2,Kida Kumiko2,Takei Junko2,Yoshida Atsushi2,Kanomata Naoki4,Kitano Atsuko5,Yamauchi Hideko2,Masuda Shinobu1

Affiliation:

1. Department of Pathology and Microbiology, Division of Oncologic Pathology Nihon University School of Medicine Tokyo Japan

2. Department of Breast Surgical Oncology St. Luke's International Hospital Tokyo Japan

3. Mammaria Tsukiji Tokyo Japan

4. Department of Pathology St. Luke's International Hospital Tokyo Japan

5. Department of Medical Oncology St Luke's International Hospital Tokyo Japan

Abstract

AbstractPregnancy‐associated breast cancer has been increasing. In this study, we analyzed patients with breast cancer that occurred during pregnancy (PrBC) and compared their genetic profiles with those of patients with breast cancer that did not occur during pregnancy, within 1 year after childbirth nor during lactation (non‐PrBC). We performed gene expression analyses of patients with PrBC and non‐PrBC using microarrays and qRT‐PCR. Microarray analysis showed that 355 genes were upregulated in the luminal‐type PrBC group compared to those in the non‐PrBC group. The C‐X‐C motif chemokine ligand 13 (CXCL13) gene was the most upregulated in the PrBC group compared to that in the non‐PrBC group, especially in the luminal A‐type (p = 0.016). This result was corroborated by the qRT‐PCR analysis of microdissected cancer cells (p < 0.001). A negative correlation was observed between CXCL13 and estrogen receptor 1 (ESR1) mRNA expression levels in luminal A‐type breast carcinoma (p < 0.001). Our results provide clues for a better understanding of breast cancer pathogenesis during pregnancy.

Funder

Japanese Breast Cancer Society

Publisher

Wiley

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