PLoS ONE (Jan 2020)

Activated leukocyte cell adhesion molecule expression correlates with the WNT subgroup in medulloblastoma and is involved in regulating tumor cell proliferation and invasion.

  • Takamune Achiha,
  • Noriyuki Kijima,
  • Yoshinori Kodama,
  • Naoki Kagawa,
  • Manabu Kinoshita,
  • Yasunori Fujimoto,
  • Masahiro Nonaka,
  • Junya Fukai,
  • Akihiro Inoue,
  • Namiko Nishida,
  • Takumi Yamanaka,
  • Atsuko Harada,
  • Kanji Mori,
  • Naohiro Tsuyuguchi,
  • Takehiro Uda,
  • Kenichi Ishibashi,
  • Yusuke Tomogane,
  • Daisuke Sakamoto,
  • Tomoko Shofuda,
  • Ema Yoshioka,
  • Daisuke Kanematsu,
  • Masayuki Mano,
  • Betty Luu,
  • Michael D Taylor,
  • Yonehiro Kanemura,
  • Haruhiko Kishima

DOI
https://doi.org/10.1371/journal.pone.0243272
Journal volume & issue
Vol. 15, no. 12
p. e0243272

Abstract

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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.