Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis.
Sclerotium rolfsii lectin (SRL) isolated from the phytopathogenic fungus Sclerotium rolfsii has exquisite binding specificity towards O-linked, Thomsen-Freidenreich (Galβ1-3GalNAcα1-Ser/Thr, TF) associated glycans. This study investigated the influence of SRL on proliferation of human breast cancer...
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Public Library of Science (PLoS)
2014-01-01
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Online Access: | http://europepmc.org/articles/PMC4217719?pdf=render |
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author | Mohammed Azharuddin Savanur Sachin M Eligar Radha Pujari Chen Chen Pravin Mahajan Anita Borges Padma Shastry Arvind Ingle Rajiv D Kalraiya Bale M Swamy Jonathan M Rhodes Lu-Gang Yu Shashikala R Inamdar |
author_facet | Mohammed Azharuddin Savanur Sachin M Eligar Radha Pujari Chen Chen Pravin Mahajan Anita Borges Padma Shastry Arvind Ingle Rajiv D Kalraiya Bale M Swamy Jonathan M Rhodes Lu-Gang Yu Shashikala R Inamdar |
author_sort | Mohammed Azharuddin Savanur |
collection | DOAJ |
description | Sclerotium rolfsii lectin (SRL) isolated from the phytopathogenic fungus Sclerotium rolfsii has exquisite binding specificity towards O-linked, Thomsen-Freidenreich (Galβ1-3GalNAcα1-Ser/Thr, TF) associated glycans. This study investigated the influence of SRL on proliferation of human breast cancer cells (MCF-7 and ZR-75), non-tumorigenic breast epithelial cells (MCF-10A) and normal mammary epithelial cells (HMECs). SRL caused marked, dose-dependent, inhibition of proliferation of MCF-7 and ZR-75 cells but only weak inhibition of proliferation of non-tumorigenic MCF-10A and HMEC cells. The inhibitory effect of SRL on cancer cell proliferation was shown to be a consequence of SRL cell surface binding and subsequent induction of cellular apoptosis, an effect that was largely prevented by the presence of inhibitors against caspases -3, -8, or -9. Lectin histochemistry using biotin-labelled SRL showed little binding of SRL to normal human breast tissue but intense binding to cancerous tissues. In conclusion, SRL inhibits the growth of human breast cancer cells via induction of cell apoptosis but has substantially less effect on normal epithelial cells. As a lectin that binds specifically to a cancer-associated glycan, has potential to be developed as an anti-cancer agent. |
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institution | Directory Open Access Journal |
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language | English |
last_indexed | 2024-12-12T16:25:15Z |
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spelling | doaj.art-57bf8f71d48e494fabfe094a86506b1d2022-12-22T00:18:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e11010710.1371/journal.pone.0110107Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis.Mohammed Azharuddin SavanurSachin M EligarRadha PujariChen ChenPravin MahajanAnita BorgesPadma ShastryArvind IngleRajiv D KalraiyaBale M SwamyJonathan M RhodesLu-Gang YuShashikala R InamdarSclerotium rolfsii lectin (SRL) isolated from the phytopathogenic fungus Sclerotium rolfsii has exquisite binding specificity towards O-linked, Thomsen-Freidenreich (Galβ1-3GalNAcα1-Ser/Thr, TF) associated glycans. This study investigated the influence of SRL on proliferation of human breast cancer cells (MCF-7 and ZR-75), non-tumorigenic breast epithelial cells (MCF-10A) and normal mammary epithelial cells (HMECs). SRL caused marked, dose-dependent, inhibition of proliferation of MCF-7 and ZR-75 cells but only weak inhibition of proliferation of non-tumorigenic MCF-10A and HMEC cells. The inhibitory effect of SRL on cancer cell proliferation was shown to be a consequence of SRL cell surface binding and subsequent induction of cellular apoptosis, an effect that was largely prevented by the presence of inhibitors against caspases -3, -8, or -9. Lectin histochemistry using biotin-labelled SRL showed little binding of SRL to normal human breast tissue but intense binding to cancerous tissues. In conclusion, SRL inhibits the growth of human breast cancer cells via induction of cell apoptosis but has substantially less effect on normal epithelial cells. As a lectin that binds specifically to a cancer-associated glycan, has potential to be developed as an anti-cancer agent.http://europepmc.org/articles/PMC4217719?pdf=render |
spellingShingle | Mohammed Azharuddin Savanur Sachin M Eligar Radha Pujari Chen Chen Pravin Mahajan Anita Borges Padma Shastry Arvind Ingle Rajiv D Kalraiya Bale M Swamy Jonathan M Rhodes Lu-Gang Yu Shashikala R Inamdar Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis. PLoS ONE |
title | Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis. |
title_full | Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis. |
title_fullStr | Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis. |
title_full_unstemmed | Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis. |
title_short | Sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis. |
title_sort | sclerotium rolfsii lectin induces stronger inhibition of proliferation in human breast cancer cells than normal human mammary epithelial cells by induction of cell apoptosis |
url | http://europepmc.org/articles/PMC4217719?pdf=render |
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