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HEG1 is a novel mucin-like membrane protein that serves as a diagnostic and therapeutic target for malignant mesothelioma.
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.
Afiliação
  • Tsuji S; Kanagawa Cancer Center Research Institute, Yokohama, Japan.
  • Washimi K; Kanagawa Cancer Center Research Institute, Yokohama, Japan.
  • Kageyama T; Department of Pathology, Kanagawa Cancer Center, Yokohama, Japan.
  • Yamashita M; Kanagawa Cancer Center Research Institute, Yokohama, Japan.
  • Yoshihara M; Kanagawa Cancer Center Research Institute, Yokohama, Japan.
  • Matsuura R; Kanagawa Cancer Center Research Institute, Yokohama, Japan.
  • Yokose T; Kanagawa Cancer Center Research Institute, Yokohama, Japan.
  • Kameda Y; Department of Pathology, Kanagawa Cancer Center, Yokohama, Japan.
  • Hayashi H; Department of Pathology, Kanagawa Cardiovascular and Respiratory Center, Yokohama, Japan.
  • Morohoshi T; Department of Pathology, Yokohama Municipal Citizen's Hospital, Yokohama, Japan.
  • Tsuura Y; Division of General Thoracic Surgery, Yokosuka-Kyosai Hospital, Yokosuka, Japan.
  • Yusa T; Division of Pathology, Yokosuka-Kyosai Hospital, Yokosuka, Japan.
  • Sato T; Department of General Thoracic Surgery and Asbestos Disease Center, Chiba Rosai Hospital, Ichihara, Japan.
  • Togayachi A; Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan.
  • Narimatsu H; Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan.
  • Nagasaki T; Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan.
  • Nakamoto K; Kanagawa Cancer Center Research Institute, Yokohama, Japan.
  • Moriwaki Y; Division of Pharmacology, Faculty of Pharmacy, Keio University, Tokyo, Japan.
  • Misawa H; Kanagawa Cancer Center Research Institute, Yokohama, Japan.
  • Hiroshima K; Division of Pharmacology, Faculty of Pharmacy, Keio University, Tokyo, Japan.
  • Miyagi Y; Division of Pharmacology, Faculty of Pharmacy, Keio University, Tokyo, Japan.
  • Imai K; Division of Pharmacology, Faculty of Pharmacy, Keio University, Tokyo, Japan.
Sci Rep ; 7: 45768, 2017 03 31.
Article em En | MEDLINE | ID: mdl-28361969
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pulmonares / Proteínas de Membrana / Mesotelioma / Anticorpos Monoclonais Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pulmonares / Proteínas de Membrana / Mesotelioma / Anticorpos Monoclonais Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article