Cancer Science

Kamlesh Guleria has completed his PhD from Guru Nanak Dev University, Amritsar, Punjab, India and Postdoctoral studies from Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne (UK). He also worked as Research Scientist at Sir Ganga Ram Hospital, New Delhi, India. Since 2009, he is working as Assistant Professor, at Department of Human Genetics Guru Nanak Dev University, Amritsar. He has published more than 20 papers in reputed journals and has  been serving as an Editorial Board Member of repute and he

has secured extramural research grants from various fundingagencies in India.

Angiogenesis is an essential process in tumor growth, provides potential routes for tumor dissemination and metastasis. Vascular endothelial growth factor (VEGF) is a potent regulator of angiogenesis and is involved in the evelopment and progression of solid tumors. Cancers use lymphangiogenesis and VEGF has been described as major mediator of breast cancer angiogenesis. The aim of the present study was to investigate the potential association of thirteen [ten promoter (-2578C/A,-2549I/D,-460T/C,-417T/C, -172C/A,-165C/T,-160C/T, -152G/A,-141A/Cand -116G/A),two 5′-UTR (+405C/G, -7C/T) and one 3′-UTR (+936C/T)] VEGF polymorphisms with breast cancer risk in patients from Punjab, North-west India. Inthis study,DNA samples of 250 pathologically confirmed breast cancer patients and 250 ages and gender matched unrelated healthy individuals were screened for thirteen selected VEGF polymorphisms using direct PCR, PCR-RFLP and Sanger sequencing methods. Of 250 breast cancer patients, 7 were males and 243 were females. About 73.6% of patients developed breast cancer after 40 years of age. A significant association of VEGF -2578AA, -2549II, -460CC, B+405GG, -152AA and -116AA genotypes with increased breast cancer risk were observed. VEGF -165CT and -141AC genotypes were associated with decreased risk for breast cancer. A strong linkage was observed between VEGF

-2578C/A and -2549I/D, -2578C/A and -460T/C,-2549I/D and -460T/C and -165C/T and -141A/C polymorphisms. Haplotype analyses indicated that EGF -2578A/-2549I/-460C/+405G/-7C/+936Cand-417T/-172C/-165C/-160C/ 152A/-141A/-116A combination was associated with increased risk while combination of -2578C/-2549D/-460T/+405G/-7C/+936C was associated with

decreased risk for breast cancer. Analysis using TFSEARCH software revealed

that VEGF -2578C/A, -417T/C, -172C/A and +405C/G polymorphisms altered

the binding site of specific transcription factors. In this case-control study, VEGF -2578C/A, -2549I/D, -460T/C, +405C/G, -165C/T, -152G/A, -141A/C and -116G/A polymorphisms were associated with susceptibility to breast cancer in patients from Punjab, North-west India. VEGF is an important target in anticancer therapy, and findings about polymorphisms influencing VEGF-targeted therapies will help physicians to tailor therapy in individual manner. Biography Kamlesh Guleria has completed his PhD from Guru Nanak Dev University, Amritsar, Punjab, India and Postdoctoral studies from Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne (UK). He also worked as ResearchScientist at Sir Ganga Ram Hospital, New Delhi, India. Since 2009, he is working as Assistant Professor, at Department of Human Genetics Guru Nanak Dev University, Amritsar. He has published more than 20 papers in reputed journals and has been serving as an Editorial Board Member of repute and he has secured extramural research grants from various funding agencies in India. guleria_k@yahoo.com mpact of functional polymorphisms of VEGF on breast cancer isk in North-west Indians amlesh Guleria1, Vasudha Sambyal1, Ruhi Kapahi1, Mridu Manjari2, eena Sudan2, Manjit Singh Uppal2 and Neeti Rajan Singh2 1Guru Nanak Dev University, India 2Sri Guru Ram Das Institute of Medical Sciences and Research, India Kamlesh Guleria et al., Arch Can Res 2018, Volume: 6 DOI: 10.21767/2254-6081-C2-008