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. 2019 Feb 26;20(2):479-485.
doi: 10.31557/APJCP.2019.20.2.479.

The Expression of Leptin and Its Receptor During Tumorigenesis of Diffuse Gliomas such as Astrocytoma and Oligodendroglioma- Grade II, III and IV (NOS)

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The Expression of Leptin and Its Receptor During Tumorigenesis of Diffuse Gliomas such as Astrocytoma and Oligodendroglioma- Grade II, III and IV (NOS)

Ramya S Vokuda et al. Asian Pac J Cancer Prev. .

Abstract

Background: Leptin, an adipocytokine functions via the leptin receptor, OB-Rb that contains an intact intracellular domain and activates the JAK/STAT signalling cascade. It stimulates growth, migration and invasion of cancer cells in vitro potentiating angiogenesis. Recently, the involvement of leptin in tumor progression is being explored. Gliomas exhibit poor prognosis, low survival rates demanding for novel therapeutic regimens resulting in discovery of many potential biomarkers and pharmaceutical targets. We analysed the potential role of leptin and OB-Rb in carcinogenesis of malignant gliomas. Methods: Sixty fresh tissue samples of diffuse gliomas were collected after tumor excision. Real time PCR, immunohistochemical (IHC) analysis and western blot analysis were carried out to assess the expression of leptin and its receptor. Results: The present study demonstrates the expression of leptin and LepR and their involvement in tumor progression. Of the 60 cases, 57 cases (95%) and 53 cases (88.3%) showed amplification for leptin and OB-Rb respectively. The expression of these proteins were measured semi-quantitatively and correlated with degree of malignancy (p<0.05). The bands were visualised on western blot. Conclusion: Leptin may be valued as a pharmaceutical target and anti-leptin compounds could be developed as drugs in mono- or combined therapies for these tumors.

Keywords: Immunohistochemistry; brain tumors; Real-time PCR.

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Conflict of interest statement

None.

Figures

Figure 1
Figure 1
Grade IV – Glioblastoma – x400 - ImmunoHistochemical Expression of Leptin
Figure 2
Figure 2
Grade IV- Glioblastoma- x400 - Immunohistochemical Expression of Leptin Receptor
Figure 3
Figure 3
Western Blot Analysis
Figure 4
Figure 4
Amplification Plot of Leptin - Real-Time PCR
Figure 5
Figure 5
Amplification Plot of Leptin Receptor– Real-Time PCR

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References

    1. Attoub S, Noe V, Pirola L, et al. Leptin promotes invasiveness of kidney and colonic epithelial cells via phosphoinositide 3-kinase, rho, and rac-dependent signaling pathways. FASEB J. 2000;14:2329–38. - PubMed
    1. Beales IL, Garcia-Morales C, Ogunwobi OO, Mutungi G. Adiponectin inhibits leptin-induced oncogenic signaling in oesophageal cancer cells by activation of PTP1B. Mol Cell Endocrinol. 2014;382:150–8. - PubMed
    1. Cheng SP, Yin PH, Hsu YC, et al. Leptin enhances migration of human papillary thyroid cancer cells through the PI3K/AKT and MEK/ERK signaling pathways. Oncol Rep. 2011;26:1265–71. - PubMed
    1. Ferla R, Bonomi M, Otvos L Jr, Surmacz E. Glioblastoma-derived leptin induces tube formation and growth of endothelial cells: comparison with VEGF effects. BMC Cancer. 2011;11:303. - PMC - PubMed
    1. Frankenberry KA, Somasundar P, McFadden DW, Vona-Davis LC. Leptin induces cell migration and the expression of growth factors in human prostate cancer cells. Am J Surg. 2004;188:560–5. - PubMed

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