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Activated leukocyte cell adhesion molecule expression correlates with the WNT subgroup in medulloblastoma and is involved in regulating tumor cell proliferation and invasion.
Achiha, Takamune; Kijima, Noriyuki; Kodama, Yoshinori; Kagawa, Naoki; Kinoshita, Manabu; Fujimoto, Yasunori; Nonaka, Masahiro; Fukai, Junya; Inoue, Akihiro; Nishida, Namiko; Yamanaka, Takumi; Harada, Atsuko; Mori, Kanji; Tsuyuguchi, Naohiro; Uda, Takehiro; Ishibashi, Kenichi; Tomogane, Yusuke; Sakamoto, Daisuke; Shofuda, Tomoko; Yoshioka, Ema; Kanematsu, Daisuke; Mano, Masayuki; Luu, Betty; Taylor, Michael D; Kanemura, Yonehiro; Kishima, Haruhiko.
Affiliation
  • Achiha T; Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Kijima N; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Kodama Y; Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Kagawa N; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Kinoshita M; Department of Neurosurgery, Osaka National Hospital, National Hospital Organization, Osaka, Japan.
  • Fujimoto Y; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Nonaka M; Department of Pathology and Applied Neurobiology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Fukai J; Department of Central Laboratory and Surgical Pathology, Osaka National Hospital, National Hospital Organization, Osaka, Japan.
  • Inoue A; Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Nishida N; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Yamanaka T; Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Harada A; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Mori K; Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Tsuyuguchi N; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Uda T; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Ishibashi K; Department of Neurosurgery, Osaka National Hospital, National Hospital Organization, Osaka, Japan.
  • Tomogane Y; Department of Neurosurgery, Kansai Medical University, Hirakata, Japan.
  • Sakamoto D; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Shofuda T; Department of Neurological Surgery, Wakayama Medical University School of Medicine, Wakayama, Japan.
  • Yoshioka E; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Kanematsu D; Department of Neurosurgery, Ehime University School of Medicine, Ehime, Japan.
  • Mano M; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Luu B; Department of Neurosurgery, Tazuke Kofukai Foundation, Medical Research Institute, Kitano Hospital, Osaka, Japan.
  • Taylor MD; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
  • Kanemura Y; Department of Neurosurgery, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Kishima H; Kansai Molecular Diagnosis Network for Central Nervous System Tumors, Osaka, Japan.
PLoS One ; 15(12): e0243272, 2020.
Article in En | MEDLINE | ID: mdl-33270750
ABSTRACT
Cluster of differentiation (CD) 166 or activated leukocyte cell adhesion molecule (ALCAM) is a transmembrane molecule known to be an intercellular adhesion factor. The expression and function of ALCAM in medulloblastoma (MB), a pediatric brain tumor with highly advanced molecular genetics, remains unclear. Therefore, this study aimed to clarify the significance and functional role of ALCAM expression in MB. ALCAM expression in 45 patients with MB was evaluated by immunohistochemical analysis of formalin-fixed paraffin-embedded clinical specimens and the relationship between ALCAM expression and pathological type/molecular subgroup, such as WNT, SHH, Group 3, and Group 4, was examined. Eight ALCAM positive (18%), seven partially positive (16%), and 30 negative (67%) cases were detected. All seven cases of the WNT molecular subgroup were ALCAM positive and ALCAM expression strongly correlated with this subgroup (P < 0.0001). In addition, functional studies using MB cell lines revealed ALCAM expression affected proliferation and migration as a positive regulator in vitro. However, ALCAM silencing did not affect survival or the formation of leptomeningeal dissemination in an orthotopic mouse model, but did induce a malignant phenotype with increased tumor cell invasion at the dissemination sites (P = 0.0029). In conclusion, our results revealed that ALCAM exhibited highly specific expression in the WNT subgroup of MB. Furthermore, we demonstrated that the cell kinetics of MB cell lines can be altered by the expression of ALCAM.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antigens, CD / Cell Adhesion Molecules, Neuronal / Wnt Proteins / Fetal Proteins / Medulloblastoma Type of study: Prognostic_studies Limits: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2020 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antigens, CD / Cell Adhesion Molecules, Neuronal / Wnt Proteins / Fetal Proteins / Medulloblastoma Type of study: Prognostic_studies Limits: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2020 Document type: Article Affiliation country: Japan
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