The role of transposable elements in aging and cancer
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作者:
Mosaddeghi, Pouria
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Shiraz Univ Med Sci, Med Plants Proc Res Ctr, Sch Pharm, Shiraz, Iran
Shiraz Univ Med Sci, Student Res Comm, Shiraz, IranShiraz Univ Med Sci, Med Plants Proc Res Ctr, Sch Pharm, Shiraz, Iran
Mosaddeghi, Pouria
[1
,2
]
Farahmandnejad, Mitra
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Shiraz Univ Med Sci, Student Res Comm, Shiraz, Iran
Shiraz Univ Med Sci, Sch Pharm, Qual Control Drug Prod Dept, Shiraz, IranShiraz Univ Med Sci, Med Plants Proc Res Ctr, Sch Pharm, Shiraz, Iran
Farahmandnejad, Mitra
[2
,3
]
Zarshenas, Mohammad M. M.
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Shiraz Univ Med Sci, Sch Pharm, Dept Phytopharmaceut Tradit Pharm, Shiraz, Iran
Shiraz Univ Med Sci, Epilepsy Res Ctr, Shiraz, IranShiraz Univ Med Sci, Med Plants Proc Res Ctr, Sch Pharm, Shiraz, Iran
Zarshenas, Mohammad M. M.
[4
,5
]
机构:
[1] Shiraz Univ Med Sci, Med Plants Proc Res Ctr, Sch Pharm, Shiraz, Iran
[2] Shiraz Univ Med Sci, Student Res Comm, Shiraz, Iran
[3] Shiraz Univ Med Sci, Sch Pharm, Qual Control Drug Prod Dept, Shiraz, Iran
Transposable elements (TEs) constitute a large portion of the human genome. Various mechanisms at the transcription and post-transcription levels developed to suppress TE activity in healthy conditions. However, a growing body of evidence suggests that TE dysregulation is involved in various human diseases, including age-related diseases and cancer. In this review, we explained how sensing TEs by the immune system could induce innate immune responses, chronic inflammation, and following age-related diseases. We also noted that inflammageing and exogenous carcinogens could trigger the upregulation of TEs in precancerous cells. Increased inflammation could enhance epigenetic plasticity and upregulation of early developmental TEs, which rewires the transcriptional networks and gift the survival advantage to the precancerous cells. In addition, upregulated TEs could induce genome instability, activation of oncogenes, or inhibition of tumor suppressors and consequent cancer initiation and progression. So, we suggest that TEs could be considered therapeutic targets in aging and cancer.
机构:
Univ Bordeaux 2, CNRS, Lab Resonance Magnet Syst Biol, UMR 5536, F-33076 Bordeaux, FranceUniv Bordeaux 2, CNRS, Lab Resonance Magnet Syst Biol, UMR 5536, F-33076 Bordeaux, France
Bringaud, Frederic
Ghedin, Elodie
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Univ Pittsburgh, Sch Med, Dept Med, Div Infect Dis, Pittsburgh, PA 15261 USAUniv Bordeaux 2, CNRS, Lab Resonance Magnet Syst Biol, UMR 5536, F-33076 Bordeaux, France
Ghedin, Elodie
El-Sayed, Najib M. A.
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机构:
Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
Univ Maryland, Ctr Bioinformat & Computat Biol, College Pk, MD 20742 USAUniv Bordeaux 2, CNRS, Lab Resonance Magnet Syst Biol, UMR 5536, F-33076 Bordeaux, France
El-Sayed, Najib M. A.
Papadopoulou, Barbara
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Univ Laval, Univ Laval Res Ctr, Ctr Hosp, Res Ctr Infect Dis, Quebec City, PQ G1V 4G2, Canada
Univ Laval, Fac Med, Dept Med Biol, Quebec City, PQ G1V 4G2, CanadaUniv Bordeaux 2, CNRS, Lab Resonance Magnet Syst Biol, UMR 5536, F-33076 Bordeaux, France