Single nucleotide polymorphism of leptin and leptin receptor genes in oral cancer - A systematic review

Authors

  • Siti Hana Ilyana Hasanbasri Kulliyyah of Dentistry, International Islamic University Malaysia, Kuantan Campus, Bandar Indera Mahkota, 25200 Kuantan, Pahang, Malaysia.
  • Nur Armidha Nadihah Amir Sabri Kulliyyah of Dentistry, International Islamic University Malaysia, Kuantan Campus, Bandar Indera Mahkota, 25200 Kuantan, Pahang, Malaysia.
  • Khairani Idah Mokhtar Department of Fundamental Dental and Medical Sciences, Kulliyyah of Dentistry, International Islamic University Malaysia, Kuantan Campus, Bandar Indera Mahkota, 25200 Kuantan, Pahang, Malaysia.
  • Basma Ezzat Mustafa Department of Fundamental Dental and Medical Sciences, Kulliyyah of Dentistry, International Islamic University Malaysia, Kuantan Campus, Bandar Indera Mahkota, 25200 Kuantan, Pahang, Malaysia.
  • Mohamad Shafiq Mohd Ibrahim Department of Paediatric Dentistry and Dental Public Health, Kulliyyah of Dentistry, International Islamic University Malaysia, Kuantan Campus, Bandar Indera Mahkota, 25200 Kuantan, Pahang, Malaysia.
  • Pram Kumar Subramaniam Department of Oral Maxillofacial Surgery and Oral Diagnosis, Kulliyyah of Dentistry, International Islamic University Malaysia, Kuantan Campus, Bandar Indera Mahkota, 25200 Kuantan, Pahang, Malaysia & Oral Dental and Maxillofacial Surgery Unit, Sultan Ahmad Shah Medical Centre, International Islamic University Malaysia, Bandar Indera Mahkota, 25200 Kuantan, Pahang, Malaysia.

DOI:

https://doi.org/10.31436/ijohs.v5i2.283

Keywords:

leptin, leptin receptor, oral cancer, oral squamous cell carcinoma, single nucleotide polymorphism

Abstract

Oral cancer is one of the serious health problems diagnosed worldwide including Malaysia. While much research has been done on the gene polymorphism of leptin and leptin receptor genes in other cancers, few researchers have considered oral cancer. Hence, this study aims to provide an insight into the association of a single nucleotide polymorphism of leptin and leptin receptor genes with oral cancer, as well as its contribution in increasing the risk for oral cancer development. Literature searches were conducted in six databases including Scopus, ScienceDirect, Web of Science, PubMed, Google Scholar, and Dimensions; focusing on articles published between 2000 to 2020. All relevant articles were screened accordingly using search terms “leptin”, “leptin receptor”, “single nucleotide polymorphism” and “oral cancer”. A total of 2699 articles were retrieved. After following the inclusion and exclusion criteria, only four articles were included in this systematic review highlighting the three commonly studied polymorphic variant of leptin and leptin receptor which are LEP -2548 G/A, LEPR Gln223Arg, and LEPR K109R. Single nucleotide polymorphism of leptin and leptin receptor genes specifically LEPR Gln223Arg and LEP -2548 G/A may increase the risk of development of oral cancer. There were limited sources available to support the findings. Further research and investigations are needed to explore the mechanism of leptin and leptin receptor genes in the development of oral cancer.

References

Ahima, R.S., & Osei, S.Y. (2004). Leptin signaling. Physiology & Behavior, 81(2), 223–241.

Atoum, M.F., Alzoughool, F., & Al-Hourani, H. (2020). Linkage between obesity leptin and breast cancer. Breast Cancer (Auckl). 14: 1178223419898458.

Domingos, P. L., Farias, L. C., Pereira, C. S., das Gracas Pena, G., Reis, T. C., Silva, R. R. et al. (2014). Leptin receptor polymorphism Gln223Arg (rs1137101) in oral squamous cell carcinoma and potentially malignant oral lesions. SpringerPlus, 3:683.

Hung, W. C., Tsai, C. M., Lin, C.W., Chuang, C. Y., Yang, S. F., & Weng, C. J. (2019). Leptin -2548 G/A polymorphisms are associated to clinical progression of oral cancer and sensitive to oral tumorization in non-smoking population. Journal of Cellular Biochemistry, 120(9), 15145-15156.

Hussain, S.R., Naqvi, H., Gupta, S., Mahdi, A. A., Kumari, P., Waseem, M., et al. (2015). A study on oncogenic role of leptin and leptin receptor in oral squamous cell. Tumour Biology, 36(8), 6515–6523.

Methley, A. M., Campbell, S., Chew-Graham, C., McNally, R., & Cheraghi-Sohi, S. (2014). PICO, PICOS and SPIDER: a comparison study of specificity and sensitivity in three search tools for qualitative systematic reviews. BMC Health Services Research, 14(579).

Rodrigues, P. R. S., Maia, L. L., Santos, M., Peterle, G. T., Alves, L. U., Takamori, J. T. et al. (2015). Leptin receptor expression and GLN223ARG polymorphism as prognostic markers in oral and oropharyngeal cancer. Genetics and Molecular Research, 14(4), 14979-14988.

Rong, G., Tang, W., Wang, Y., Qiu, H., & Chen, S. (2019). Investigation of leptin receptor RS1137101 G>A polymorphism with cancer risk: Evidence from 35936 subjects. Bioscience Reports, 39(6): BSR20182240.

Sobrinho Santos, E. M., Guimaraes, T. A., Santos, H. O., Cangussu, L. M., de Jesus, S. F., Fraga, C. A. et al., (2017). Leptin acts on neoplastic behaviour and expression levels of genes related to hypoxia, angiogenesis, and invasiveness in oral squamous cell carcinoma. Tumor Biology, 39(5):1010428317699130.

Tilg, H., & Moschen, A. (2006). Adipocytokines: mediators linking adipose tissue, inflammation and immunity. Nature Reviews Immunology, 6(10), 772–783.

Yang, Y., & Niu, T. (2018). A meta-analysis of associations of LEPR Q223R and K109R polymorphisms with type 2 diabetes risk. PLoS One,13(1): e0189366.

Yapijakis, C., Kechagiadakis, M., Nkenke, E., Serefoglou, Z., Avgoustidis, D., Vylliotis, A. et al. (2009). Association of leptin -2548G/A and leptin receptor Q223R polymorphisms with increased risk for oral cancer. Journal of Cancer Research and Clinical Oncology, 135(4), 603-612.

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Published

2024-07-31

How to Cite

Hasanbasri, S. H. I. ., Amir Sabri, N. A. N. ., Mokhtar, K. I., Ezzat Mustafa, B. ., Mohd Ibrahim, M. S. ., & Subramaniam, P. K. . (2024). Single nucleotide polymorphism of leptin and leptin receptor genes in oral cancer - A systematic review. IIUM Journal of Orofacial and Health Sciences, 5(2), 164–172. https://doi.org/10.31436/ijohs.v5i2.283

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