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    <subfield code="a">Cai01.12.02.Ph.D.2021.Ma.E.</subfield>
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    <subfield code="a">Mahmod Morad Ragab Mohammed,</subfield>
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    <subfield code="a">Expression and polymorphism of long non-coding RNAs in colorectal cancer / </subfield>
    <subfield code="c">Mahmod Morad Ragab Mohammed ; Supervised Prof.Dr. Ismail Abdelshafy Abdelhamid , Prof.Dr.Heba Mohammed Kamal Abdelhakeem , Prof.Dr.Olfat Gamil Shaker.</subfield>
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    <subfield code="a">84 Pages : </subfield>
    <subfield code="b">charts , facsimiles ; </subfield>
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    <subfield code="a">Bibliography: pages 115-137.</subfield>
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    <subfield code="a">Background: Colorectal cancer (CRC) is a complex disease that develops as a consequence of both genetic and environmental risk factors. Diet, smoking and drinking habits are among environmental factors frequently associated with CRC risk. Aim of work:The present study aims to conduct a clinical biochemical study that aids in the investigation of some non-coding RNA expressions and polymorphisms (including long non-coding RNAs and miRNAs) namely, Plasmacytoma Variant Translocation-1 (PVT-1) and miR-186 in an attempt to provide new noninvasive diagnostic biomarkers for CRC of the Egyptian patients. Patients and methods: Eighty CRC studies and thirty healthy controls were included. Laboratory and pathological investigations were assessed. Serum miR-186 and long non-coding PVT-1 was measured as well as genotype for PVT-1 rs13255292. Results: The CRC patients had a mean age of 50.91&#xB1;12.0. The mean serum miR-186 level in CRC patients (1.38&#xB1;0.21) was significantly higher than in the control (0.93&#xB1;0.1) (p=0.0001). The PVT-1 level in CRC patients was (5.91&#xB1;0.25) significantly higher than control (1.1&#xB1;0.2) (p=0.001). The PVT-1/ rs13255292 genotype CT was significantly higher compared to the control group. The T allele was highly significant with a p-value of 0.008 in the CRC patient group with respect to the control. Conclusion: miR-186, long noncoding PVT-1 as well as PVT-1 the T allele may be considered as genetic markers for CRC susceptibility</subfield>
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    <subfield code="a">Issued also as CD</subfield>
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    <subfield code="a">Text in English and abstract in Arabic &amp; English.</subfield>
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    <subfield code="a">Biochemistry </subfield>
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    <subfield code="a">Colorectal Cancer (CRC)</subfield>
    <subfield code="a">Long non-coding RNAs (lncRNAs)</subfield>
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    <subfield code="a">Heba Mohammed Kamal Abdelhakeem </subfield>
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    <subfield code="a">Ismail Abd Elshafy Abd Elhamid </subfield>
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    <subfield code="a">Olfat Gamil Shaker </subfield>
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    <subfield code="b">01-01-2022</subfield>
    <subfield code="c">Ismail Abdelshafy Abdelhamid</subfield>
    <subfield code="c">Heba Mohammed Kamal Abdelhakeem </subfield>
    <subfield code="c">Olfat Gamil Shaker</subfield>
    <subfield code="U">Cairo University </subfield>
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