Immunophenotypic signature of primary glioblastoma multiforme: A case of extended progression free survival

doi:10.12998/wjcc.v5.i6.247

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World Journal of Clinical Cases

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Jun 16, 2017; 5(6): 247-253
Published online Jun 16, 2017. doi: 10.12998/wjcc.v5.i6.247

Table 2 Parameters evaluated in circulation (serum/plasma)

No.	Case/group	NLR	hTERT	YKL-40	TIMP-1	¹IL-6	²HMGA1
1	Case	3.9	6.125	71.47	80	645.207	16.8
2	Control (n = 15)	1.6 (0.87-28)	1.14 (0.22-1.585)	18.3 (1.12-66.7)	23.7 (10.3-88.4)	48.9 (6.71-72.8)	-
3	GBM (n = 30)	5.58 (3.1-18)	2.18 (0.565-8.84)	101.2 (21.2-198.8)	93.8 (37.2-185.1)	197.6 (59.2-803.7)	30.613

¹n = 15; hTERT, TIMP-1 and YKL-40, IL-6 quantified in ng/L, ng/mL and pg/mL respectively;

²HMGA1 quantified in terms of protein band density. NLR: Neutrophil lymphocyte ratio; HMGA1: High mobility group-A1; hTERT: Human telomerase reverse transcriptase; IL-6: Interleukin-6; TIMP-1: Tissue inhibitor of metalloproteinases-1; YKL-40: Human chitinase-3-like-protein-1.

Citation: Gandhi P, Khare R, Garg N, Sorte S. Immunophenotypic signature of primary glioblastoma multiforme: A case of extended progression free survival. World J Clin Cases 2017; 5(6): 247-253
URL: https://www.wjgnet.com/2307-8960/full/v5/i6/247.htm
DOI: https://dx.doi.org/10.12998/wjcc.v5.i6.247