Literature DB >> 19451095

Differences in mRNA and microRNA microarray expression profiles in human colon adenocarcinoma HT-29 cells treated with either Intensity-modulated Radiation Therapy (IMRT), or Conventional Radiation Therapy (RT).

Farid E Ahmed1, Paul W Vos, Clark Jeffries, John E Wiley, Douglas A Weidner, Helvecio Mota, Chris Bonnerup, Claudio Sibata, Ron R Allison.   

Abstract

We carried out this in vitro molecular study to investigate the effect of two clinical X-irradiation modalities (a two-dimensional external beam radiotherapy referred to in this article as conventional RT, and a three dimensional conformal intensity-modulated radiation therapy (IMRT) on a colon adenocarcinoma HT-29 cell line. Cells were synchronized by serum deprivation 48 h before irradiation so that >90% of them were in the G(0)/G(1) phase of the cell cycle. Cells were allowed to recover 3 h after irradiation before total RNA extraction. Two types of arrays, namely Affymetrix Human HG U133A 2.0 oligonucleotide microarrays and Ambion mirVana bioarrays, were employed to study mRNA and microRNA expressions, respectively. Three flasks were used per irradiation dose, and an additional three unirradiated flasks served as control. Microarray data were validated by reverse transcriptase quantitative polymerase chain reaction, and proteins of some expressed genes were determined by Western blots. Results showed the existence of differences in expression profiles between the two irradiation modalities. IMRT appeared to influence expression of some DNA repair genes, whereas in conventional RT, some DNA repair and cell cycle-related genes that initially seemed to be preferentially expressed dwindled to normal levels. Earlier in vitro experiments using cell survival to study sublethal damage repair support our conclusions. Bioinformatic investigation revealed a correlation of gene expression with derepression effects of microRNA molecules. We have presented opinions as to how microRNAs might influence gene expression during radiation-induced stress and have suggested future avenues for research.

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Year:  2009        PMID: 19451095

Source DB:  PubMed          Journal:  Cancer Genomics Proteomics        ISSN: 1109-6535            Impact factor:   4.069


  8 in total

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Authors:  Michael Hollis; Kavitha Nair; Arpita Vyas; Lakshmi Shankar Chaturvedi; Sahil Gambhir; Dinesh Vyas
Journal:  World J Gastroenterol       Date:  2015-07-21       Impact factor: 5.742

2.  Simultaneous profiling of 194 distinct receptor transcripts in human cells.

Authors:  Byong H Kang; Karin J Jensen; Jaime A Hatch; Kevin A Janes
Journal:  Sci Signal       Date:  2013-08-06       Impact factor: 8.192

Review 3.  Serum microRNAs: A new diagnostic method for colorectal cancer.

Authors:  Yi Yang; Xiaodong Gu; Minwei Zhou; Jianbin Xiang; Zongyou Chen
Journal:  Biomed Rep       Date:  2013-05-20

Review 4.  MicroRNA dysregulation in colorectal cancer: a clinical perspective.

Authors:  Y Dong; W K K Wu; C W Wu; J J Y Sung; J Yu; S S M Ng
Journal:  Br J Cancer       Date:  2011-03-01       Impact factor: 7.640

5.  Cellular stress induced alterations in microRNA let-7a and let-7b expression are dependent on p53.

Authors:  Anthony D Saleh; Jason E Savage; Liu Cao; Benjamin P Soule; David Ly; William DeGraff; Curtis C Harris; James B Mitchell; Nicole L Simone
Journal:  PLoS One       Date:  2011-10-11       Impact factor: 3.240

6.  Cross-Resistance of Acquired Radioresistant Colorectal Cancer Cell Line to gefitinib and regorafenib.

Authors:  Saeid Afshar; Abdolazim Sedighi Pashaki; Rezvan Najafi; Safoora Nikzad; Razieh Amini; Nooshin Shabab; Omid Khiabanchian; Hamid Tanzadehpanah; Massoud Saidijam
Journal:  Iran J Med Sci       Date:  2020-01

7.  MicroRNA-148b enhances the radiosensitivity of non-Hodgkin's Lymphoma cells by promoting radiation-induced apoptosis.

Authors:  Yong Wu; Guo-Long Liu; Si-Hong Liu; Cai-Xia Wang; Yan-Li Xu; Yi Ying; Ping Mao
Journal:  J Radiat Res       Date:  2012-06-06       Impact factor: 2.724

8.  Differential miRNA expression profiling reveals miR-205-3p to be a potential radiosensitizer for low- dose ionizing radiation in DLD-1 cells.

Authors:  Rodrigo Andaur; Julio C Tapia; José Moreno; Leopoldo Soto; Ricardo Armisen; Katherine Marcelain
Journal:  Oncotarget       Date:  2018-05-29
  8 in total

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