Unknown

Dataset Information

0

YKL-40 protein expression in human tumor samples and human tumor cell line xenografts: implications for its use in tumor models.


ABSTRACT:

Background

YKL-40, also known as non-enzymatic chitinase-3 like-protein-1 (CHI3L1), is a glycoprotein expressed and secreted mainly by inflammatory cells and tumor cells. Accordingly, several studies demonstrated elevated YKL-40 serum levels in cancer patients and found YKL-40 to be correlated with a poor prognosis and disease severity in some tumor entities. YKL-40 was suggested to be involved in angiogenesis and extracellular matrix remodeling. As yet, however, its precise biological function remains elusive.

Methods

As YKL-40 protein expression has only been investigated in few malignancies, we employed immunohistochemical detection in a large multi-tumor tissue microarray consisting of 2,310 samples from 72 different tumor entities. In addition, YKL-40 protein expression was determined in primary mouse xenograft tumors derived from human cancer cell lines.

Results

YKL-40 could be detected in almost all cancer entities and was differently expressed depending on tumor stage and subtype (e.g., thyroid cancer, colorectal cancer, gastric cancer and ovarian cancer). While YKL-40 was absent in in vitro grown human cancer cell lines, YKL-40 expression was upregulated in xenograft tumor tissues in vivo.

Conclusions

These data provide new insights into YKL-40 expression at the protein level in various tumor entities and its regulation in tumor models. Our data suggest that upregulation of YKL-40 expression is a common feature in vivo and is finely regulated by tumor cell-microenvironment interactions.

SUBMITTER: Bockelmann LC 

PROVIDER: S-EPMC8516773 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC7603212 | biostudies-literature
| S-EPMC2795793 | biostudies-literature
| S-EPMC6351153 | biostudies-literature
| S-EPMC7180208 | biostudies-literature
| S-EPMC3908752 | biostudies-literature
| S-EPMC3091949 | biostudies-literature
| S-EPMC4355396 | biostudies-literature
| S-EPMC3559234 | biostudies-literature
| S-EPMC5967238 | biostudies-literature
2024-09-10 | GSE217590 | GEO