scholarly journals The variability of multi-drug resistance ABCB1 gene in the Roma population from Croatia

2019 ◽  
Vol 2 (1) ◽  
pp. 10-18
Author(s):  
Matea Zajc Petranovic ◽  
Zeljka Tomas ◽  
Tatjana Skaric-Juric ◽  
Nina Smolej Narancic ◽  
Branka Janicijevic ◽  
...  

When overexpressed, a large transmembrane P-glycoprotein, the product of the ABCB1 gene, is a notable impediment to brain-targeted therapies (like antiepileptics) and chemotherapies. Some of the genetic biomarkers with evidence of multi-drug resistance in ABCB1 ― rs1045642, rs1128503, and rs3213619 ― were analyzed in 440 subjects, members of three socio-culturally different Roma (Gypsy) groups of Croatia. Minor allele frequencies (MAFs) of rs1045642 and rs1128503 were the highest in the Balkan Roma (63.6% and 69.4%, respectively) when compared to the Baranja (52.3% and 62.5%) and the Međimurje Roma (48.8% and 54.5%) (p=0.0005 and p=0.0011, respectively). rs3213619 was monomorphic in the Međimurje group, while its MAFs in other two Roma groups were very low (<1.9%). The distribution of five detected haplotypes (four in the Međimurje group) significantly differed between the Roma subpopulations (p<0.0001), just like the frequencies of diplotypes (p=0.0008). At a global scale, the positive relationship between genetic and geographic distances between the 21 investigated populations indicates isolation by spatial distance. However, this is not true for the relationship between Roma and other populations due to their population history. The analyzed ABCB1 loci indicate genetic distinctiveness of the Roma population.

Heterocycles ◽  
2015 ◽  
Vol 90 (1) ◽  
pp. 482
Author(s):  
Takayuki Doi ◽  
Naoko Yamaguchi ◽  
Kosuke Ohsawa ◽  
Kazuoki Nakai ◽  
Masahito Yoshida ◽  
...  

Oncotarget ◽  
2015 ◽  
Vol 6 (28) ◽  
pp. 26308-26321 ◽  
Author(s):  
Abhilash K. Ravindranath ◽  
Swayamjot Kaur ◽  
Roman P. Wernyj ◽  
Muthu N. Kumaran ◽  
Karl E. Miletti-Gonzalez ◽  
...  

Open Biology ◽  
2012 ◽  
Vol 2 (5) ◽  
pp. 120066 ◽  
Author(s):  
Piet Borst

Although chemotherapy of tumours has scored successes, drug resistance remains the major cause of death of cancer patients. Initial treatment often leaves residual disease, from which the tumour regrows. Eventually, most tumours become resistant to all available chemotherapy. I call this pan-resistance to distinguish it from multi-drug resistance, usually describing resistance caused by upregulation of drug transporters, such as P-glycoprotein. In this review, I discuss mechanisms proposed to explain both residual disease and pan-resistance. Although plausible explanations are at hand for residual disease, pan-resistance is still a mystery. My conclusion is that it is time for a major effort to solve this mystery using the new genetically modified mouse tumour models that produce real tumours resembling cancer in human patients.


1995 ◽  
Vol 16 (4) ◽  
pp. 253-257 ◽  
Author(s):  
J. R. BALLINGER ◽  
H. A. HUA ◽  
B. W. BERRY ◽  
P. FIRBY ◽  
I. BOXEN

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