Expression analysis of HMGB1 in histological samples of malignant pleural mesothelioma

被引:17
|
作者
Rrapaj, Eltjona [1 ]
Trisolini, Elena [1 ]
Bertero, Luca [2 ]
Salvo, Michela [1 ]
Indellicato, Rossella [1 ]
Andorno, Silvano [1 ]
Garcia-Manteiga, Jose M. [3 ]
Rena, Ottavio [4 ]
Boldorini, Renzo L. [1 ,5 ]
机构
[1] Univ Piemonte Orientale, Dept Hlth Sci, Via Solaroli 17, I-28100 Novara, Italy
[2] Univ Turin, Dept Med Sci, Div Pathol, Turin, Italy
[3] IRCCS San Raffaele Hosp, Ctr Translat Genom & Bioinformat, Milan, Italy
[4] Maggiore della Carita Hosp, Unit Thorac Surg, Novara, Italy
[5] Maggiore della Carita Hosp, Unit Pathol, Novara, Italy
关键词
biomarker; high mobility group box 1; histological samples; malignant pleural mesothelioma; prognosis; GROUP BOX 1; MOBILITY GROUP BOX-1; REGULATES AUTOPHAGY; ASBESTOS EXPOSURE; COLORECTAL-CANCER; CHROMATIN PROTEIN; GENE-EXPRESSION; CELL; CARCINOMA; CARCINOGENESIS;
D O I
10.1111/his.13470
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
AimsHigh mobility group box 1 (HMGB1) is a chromatin structural protein, expressed ubiquitously in the nuclei of mammalian cells. When transported extracellularly, it acts as a tumour suppressor and oncogenic protein. In malignant pleural mesothelioma (MPM), high serum levels of HMGB1 have been related to a poor prognosis. Conversely, the significance of HMGB1 expression in MPM tissues is still unclear. Methods and resultsBiopsy samples from 170 patients with MPM were assessed by immunohistochemistry and reverse transcription-polymerase chain reaction (RT-PCR) to evaluate HMGB1 protein and gene expression. The expression level of HMGB1 protein was scored using a semiquantitative system that sums the intensity (0-3) and the percentage (from 0 to 4) of positively stained cells in nuclei, cytoplasm and in both. The final score was considered as high (>3) or low (<3) expression. Gene expression levels were calculated using the C-t method. High expression levels of HMGB1 as total (P = 0.0011) and cytoplasmic score (P = 0.0462) were related to a worse disease-specific survival (DSS) in the entire cohort and in the clinicopathological subgroups. No significant correlation was found between HMGB1 gene expression and DSS. ConclusionsThese findings indicate that HMGB1 may be a useful prognostic biomarker in MPM when detected by immunohistochemistry. Conversely, as it is also expressed in normal and reactive mesothelial cells, HMGB1 cannot be considered a diagnostic biomarker in histological samples of mesothelioma.
引用
收藏
页码:1039 / 1050
页数:12
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