TY - JOUR
T1 - ATRX protein loss and deregulation of PI3K/AKT pathway is frequent in pilocytic astrocytoma with anaplastic features
AU - Olar, Adriana
AU - Tran, Diep
AU - Mehta, Vidya P.
AU - Reinhardt, Annekathrin
AU - Manekia, Jawad H.
AU - Garnovskaya, Maria
AU - Ellezam, Benjamin
AU - Luthra, Rajyalakshmi
AU - Sulman, Erik P.
AU - Mohila, Carrie A.
AU - Campbell, Gerald A.
AU - Powell, Suzanne Zein-Eldin
AU - Fuller, Gregory N.
AU - Aldape, Kenneth D.
AU - Adesina, Adekunle M.
N1 - Publisher Copyright:
©2019 Dustri-Verlag Dr. K. Feistle.
PY - 2019/3/1
Y1 - 2019/3/1
N2 - Introduction: Pilocytic astrocytoma (PA) with anaplastic features (PAAF) is a rare entity associated with decreased survival. It is characterized by hypercellularity, atypia, brisk mitotic activity, variable necrosis, and association with a classic PA component or anaplastic transformation in a recurrent tumor with a previously-documented classic PA. Materials and methods: We present 5 PAAF cases with clinical, radiological, pathological, and molecular correlation. We interrogated ATRX, IDH, TP53, PTEN, EGFR, BRAF, 6q23, p16(Ink4a) by sequencing, FISH, and immunohistochemistry. Results: Four tumors were located in the cerebellum, and 1 was supratentorial. All showed ATRX protein loss by immunohistochemistry, loss of heterozygosity for PTEN, and had no IDH/TP53/BRAF mutations, nor EGFR amplification. Two of 5 tumors showed BRAF duplication by pyrosequencing. All showed loss of PTEN nuclear expression in subsets of tumor cells, which was associated with variable cytoplasmic positivity for pS6. There was a relative correlation between loss of PTEN expression and pS6 cytoplasmic expression. p53 was expressed in ~ 50% of tumor cells in all tumors. P16 was variably lost in all cases. One tumor showed MYB/6q23 deletion. Conclusion: We confirm ATRX protein loss suggestive of ATRX alteration as well as dysregulation of the PI3K/AKT pathway and, less often, of the MAPK/ERK pathway in PAAF.
AB - Introduction: Pilocytic astrocytoma (PA) with anaplastic features (PAAF) is a rare entity associated with decreased survival. It is characterized by hypercellularity, atypia, brisk mitotic activity, variable necrosis, and association with a classic PA component or anaplastic transformation in a recurrent tumor with a previously-documented classic PA. Materials and methods: We present 5 PAAF cases with clinical, radiological, pathological, and molecular correlation. We interrogated ATRX, IDH, TP53, PTEN, EGFR, BRAF, 6q23, p16(Ink4a) by sequencing, FISH, and immunohistochemistry. Results: Four tumors were located in the cerebellum, and 1 was supratentorial. All showed ATRX protein loss by immunohistochemistry, loss of heterozygosity for PTEN, and had no IDH/TP53/BRAF mutations, nor EGFR amplification. Two of 5 tumors showed BRAF duplication by pyrosequencing. All showed loss of PTEN nuclear expression in subsets of tumor cells, which was associated with variable cytoplasmic positivity for pS6. There was a relative correlation between loss of PTEN expression and pS6 cytoplasmic expression. p53 was expressed in ~ 50% of tumor cells in all tumors. P16 was variably lost in all cases. One tumor showed MYB/6q23 deletion. Conclusion: We confirm ATRX protein loss suggestive of ATRX alteration as well as dysregulation of the PI3K/AKT pathway and, less often, of the MAPK/ERK pathway in PAAF.
KW - Anaplastic
KW - MAPK/ERK
KW - MYB-ATRX
KW - PI3K/AKT
KW - Pilocytic astrocytoma
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U2 - 10.5414/NP301105
DO - 10.5414/NP301105
M3 - Article
C2 - 30499772
AN - SCOPUS:85061970131
SN - 0722-5091
VL - 38
SP - 59
EP - 73
JO - Clinical neuropathology
JF - Clinical neuropathology
IS - 2
ER -