ITLN1 modulates invasive potential and metabolic reprogramming of ovarian cancer cells in omental microenvironment

Advanced ovarian cancer usually spreads to the omentum. However, the omental cell-derived molecular determinants modulating its progression have not been thoroughly characterized. Here, we show that circulating ITLN1 has prognostic significance in patients with advanced ovarian cancer. Further studi...

Full description

Saved in:
Bibliographic Details
Published inNature communications Vol. 11; no. 1; pp. 3546 - 16
Main Authors Au-Yeung, Chi-Lam, Yeung, Tsz-Lun, Achreja, Abhinav, Zhao, Hongyun, Yip, Kay-Pong, Kwan, Suet-Ying, Onstad, Michaela, Sheng, Jianting, Zhu, Ying, Baluya, Dodge L., Co, Ngai-Na, Rynne-Vidal, Angela, Schmandt, Rosemarie, Anderson, Matthew L., Lu, Karen H., Wong, Stephen T. C., Nagrath, Deepak, Mok, Samuel C.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 15.07.2020
Nature Publishing Group
Nature Portfolio
Subjects
Online AccessGet full text
ISSN2041-1723
2041-1723
DOI10.1038/s41467-020-17383-2

Cover

More Information
Summary:Advanced ovarian cancer usually spreads to the omentum. However, the omental cell-derived molecular determinants modulating its progression have not been thoroughly characterized. Here, we show that circulating ITLN1 has prognostic significance in patients with advanced ovarian cancer. Further studies demonstrate that ITLN1 suppresses lactotransferrin’s effect on ovarian cancer cell invasion potential and proliferation by decreasing MMP1 expression and inducing a metabolic shift in metastatic ovarian cancer cells. Additionally, ovarian cancer-bearing mice treated with ITLN1 demonstrate marked decrease in tumor growth rates. These data suggest that downregulation of mesothelial cell-derived ITLN1 in the omental tumor microenvironment facilitates ovarian cancer progression. Advanced ovarian cancer usually spreads to the omentum. Here, the authors show that circulating intelectin-1 (ITLN1) has prognostic significance in patients with advanced ovarian cancer, and that mesothelial cell-derived ITLN1 in the omental tumor microenvironment suppresses ovarian cancer progression.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ObjectType-Undefined-3
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-020-17383-2