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HEG1 is a novel mucin-like membrane protein that serves as a diagnostic and therapeutic target for malignant mesothelioma

The absence of highly specific markers for malignant mesothelioma (MM) has served an obstacle for its diagnosis and development of molecular-targeting therapy against MM. Here, we show that a novel mucin-like membrane protein, sialylated protein HEG homolog 1 (HEG1), is a highly specific marker for...

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Detalles Bibliográficos
Autores principales: Tsuji, Shoutaro, Washimi, Kota, Kageyama, Taihei, Yamashita, Makiko, Yoshihara, Mitsuyo, Matsuura, Rieko, Yokose, Tomoyuki, Kameda, Yoichi, Hayashi, Hiroyuki, Morohoshi, Takao, Tsuura, Yukio, Yusa, Toshikazu, Sato, Takashi, Togayachi, Akira, Narimatsu, Hisashi, Nagasaki, Toshinori, Nakamoto, Kotaro, Moriwaki, Yasuhiro, Misawa, Hidemi, Hiroshima, Kenzo, Miyagi, Yohei, Imai, Kohzoh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374711/
https://www.ncbi.nlm.nih.gov/pubmed/28361969
http://dx.doi.org/10.1038/srep45768
Descripción
Sumario:The absence of highly specific markers for malignant mesothelioma (MM) has served an obstacle for its diagnosis and development of molecular-targeting therapy against MM. Here, we show that a novel mucin-like membrane protein, sialylated protein HEG homolog 1 (HEG1), is a highly specific marker for MM. A monoclonal antibody against sialylated HEG1, SKM9-2, can detect even sarcomatoid and desmoplastic MM. The specificity and sensitivity of SKM9-2 to MM reached 99% and 92%, respectively; this antibody did not react with normal tissues. This accurate discrimination by SKM9-2 was due to the recognition of a sialylated O-linked glycan with HEG1 peptide. We also found that gene silencing of HEG1 significantly suppressed the survival and proliferation of mesothelioma cells; this result suggests that HEG1 may be a worthwhile target for function-inhibition drugs. Taken together, our results indicate that sialylated HEG1 may be useful as a diagnostic and therapeutic target for MM.