Unknown

Dataset Information

0

Involvement of highly sulfated chondroitin sulfate in the metastasis of the Lewis lung carcinoma cells.


ABSTRACT: The altered expression of cell surface chondroitin sulfate (CS) and dermatan sulfate (DS) in cancer cells has been demonstrated to play a key role in malignant transformation and tumor metastasis. However, the functional highly sulfated structures in CS/DS chains and their involvement in the process have not been well documented. In the present study, a structural analysis of CS/DS from two mouse Lewis lung carcinoma (3LL)-derived cell lines with different metastatic potentials revealed a higher proportion of Delta(4,5)HexUA-GalNAc(4,6-O-disulfate) generated from E-units (GlcUA-GalNAc(4, 6-O-disulfate)) in highly metastatic LM66-H11 cells than in low metastatic P29 cells, although much less CS/DS is expressed by LM66-H11 than P29 cells. This key finding prompted us to study the role of CS-E-like structures in experimental lung metastasis. The metastasis of LM66-H11 cells to lungs was effectively inhibited by enzymatic removal of tumor cell surface CS or by preadministration of CS-E rich in E-units in a dose-dependent manner. In addition, immunocytochemical analysis showed that LM66-H11 rather than P29 cells expressed more strongly the CS-E epitope, which was specifically recognized by the phage display antibody GD3G7. More importantly, this antibody and a CS-E decasaccharide fraction, the minimal structure recognized by GD3G7, strongly inhibited the metastasis of LM66-H11 cells probably by modifying the proliferative and invading behavior of the metastatic tumor cells. These results suggest that the E-unit-containing epitopes are involved in the metastatic process and a potential target for the diagnosis and treatment of malignant tumors.

SUBMITTER: Li F 

PROVIDER: S-EPMC2662238 | biostudies-literature | 2008 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Involvement of highly sulfated chondroitin sulfate in the metastasis of the Lewis lung carcinoma cells.

Li Fuchuan F   Ten Dam Gerdy B GB   Murugan Sengottuvelan S   Yamada Shuhei S   Hashiguchi Taishi T   Mizumoto Shuji S   Oguri Kayoko K   Okayama Minoru M   van Kuppevelt Toin H TH   Sugahara Kazuyuki K  

The Journal of biological chemistry 20081016 49


The altered expression of cell surface chondroitin sulfate (CS) and dermatan sulfate (DS) in cancer cells has been demonstrated to play a key role in malignant transformation and tumor metastasis. However, the functional highly sulfated structures in CS/DS chains and their involvement in the process have not been well documented. In the present study, a structural analysis of CS/DS from two mouse Lewis lung carcinoma (3LL)-derived cell lines with different metastatic potentials revealed a higher  ...[more]

Similar Datasets

| S-EPMC6405089 | biostudies-literature
| S-EPMC8430715 | biostudies-literature
| S-EPMC1876374 | biostudies-literature
| S-EPMC4949442 | biostudies-literature
| PRJNA578483 | ENA
2020-02-01 | GSE139120 | GEO
| S-EPMC3230280 | biostudies-literature
| S-EPMC4938203 | biostudies-literature
2010-09-06 | GSE18244 | GEO
2010-09-06 | E-GEOD-18244 | biostudies-arrayexpress