This study investigated the relationship between a polymorphism (rs1800857 T/C) of the Cholecystokinin type A receptor (CCKAR) gene and gallstone disease susceptibility. The researchers genotyped 502 subjects (272 gallstone patients and 230 controls) and analyzed CCKAR expression levels in gallbladder tissue samples. They found that the C allele of the CCKAR polymorphism was associated with increased gallstone disease risk. CCKAR expression was also higher in gallbladder tissues from patients with the C allele compared to those with the T allele.
This study investigated the relationship between a polymorphism (rs1800857 T/C) of the Cholecystokinin type A receptor (CCKAR) gene and gallstone disease susceptibility. The researchers genotyped 502 subjects (272 gallstone patients and 230 controls) and analyzed CCKAR expression levels in gallbladder tissue samples. They found that the C allele of the CCKAR polymorphism was associated with increased gallstone disease risk. CCKAR expression was also higher in gallbladder tissues from patients with the C allele compared to those with the T allele.
This study investigated the relationship between a polymorphism (rs1800857 T/C) of the Cholecystokinin type A receptor (CCKAR) gene and gallstone disease susceptibility. The researchers genotyped 502 subjects (272 gallstone patients and 230 controls) and analyzed CCKAR expression levels in gallbladder tissue samples. They found that the C allele of the CCKAR polymorphism was associated with increased gallstone disease risk. CCKAR expression was also higher in gallbladder tissues from patients with the C allele compared to those with the T allele.
Received: 16 December 2015 / Accepted: 27 May 2016
! Springer Science+Business Media New York 2016
Abstract In the present study, we investigated expression pattern of Cholecys-
tokinin type A receptor (CCKAR) in relation to its commonly studied polymor- phism (rs1800857, T/C) in gallstone disease (GSD) patients and controls. A total of 502 subjects (272 GSD and 230 controls) were enrolled, and genotyping was per- formed by evaluating restriction fragments of PstI digested DNA. For analyzing expression pattern of CCKAR in relation to polymorphism, gallbladder tissue
& Abhijit Chandra
abhijitchandra@hotmail.com Hasan Raza Kazmi hasanrazakazmi@yahoo.co.in Jaya Nigam jayanigam27@gmail.com Kavita Baghel kavita.baghel08@gmail.com Meenu Srivastava meenu.srivastava12@gmail.com Shailendra S. Maurya shailendrabt@gmail.com Devendra Parmar parmar_devendra1@rediffmail.com 1 Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi 221005, India 2 Department of Surgical Gastroenterology, King George’s Medical University, Lucknow 226003, India 3 Developmental Toxicology Division, Indian Institute of Toxicology Research, Lucknow 226003, India
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