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Chitinase 3-Like 2.
Nimbalkar, Vidya P; Kruthika, Banavathy S; Sravya, Palavalasa; Rao, Shilpa; Sugur, Harsha S; Chickabasaviah, Yasha T; Somanna, Sampath; Arivazhagan, Arimappamagan; Kondaiah, Paturu; Santosh, Vani.
Afiliação
  • Nimbalkar VP; Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
  • Kruthika BS; Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
  • Sravya P; Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
  • Rao S; Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
  • Sugur HS; Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
  • Chickabasaviah YT; Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
  • Somanna S; Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore, India.
  • Arivazhagan A; Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore, India.
  • Kondaiah P; Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bangalore, India.
  • Santosh V; Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
Am J Clin Pathol ; 158(4): 521-529, 2022 10 06.
Article em En | MEDLINE | ID: mdl-35913110
ABSTRACT

OBJECTIVES:

We aimed to evaluate the expression pattern of chitinase 3-like 2 (CHI3L2) in the tumor core and peritumoral brain zone (PBZ) of newly diagnosed glioblastoma (GBM) in recurrent tumors and its association with patient prognosis.

METHODS:

The study was conducted on three sample sets derived from different patient cohorts. Messenger RNA (mRNA) expression of CHI3L2 in the tumor core and PBZ (n = 34) compared with control (n = 20) tissues was studied by quantitative polymerase chain reaction in sample set 1. Sample set 2 included 19 paired, primary-recurrent GBM tissues. Sample set 3 comprised 82 GBM tissues of patients with treatment and follow-up information. Immunohistochemistry (IHC) was performed on all three sample sets.

RESULTS:

mRNA expression of CHI3L2 was significantly higher in the tumor core and PBZ compared with control (P < .0001). By IHC, CHI3L2 showed strong cytoplasmic staining in tumor cells. Recurrent tumors had a higher expression of CHI3L2 compared with primary tumors (P = .007). Survival analysis showed CHI3L2 expression was associated with shorter overall survival (P = .034) and progression-free survival (P = .010), which was in line with The Cancer Genome Atlas cohort (P = .043).

CONCLUSIONS:

High expression of CHI3L2 in the tumor core and PBZ, as well as its association with tumor recurrence and poor patient prognosis, suggests it might be contributing to tumor spread and recurrence.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Quitinases / Glioblastoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Quitinases / Glioblastoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article