Expression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer.
<h4>Background</h4>MicroRNA expression is severely disrupted in carcinogenesis, however limited evidence is available validating results from cell-line models in human clinical cancer specimens. MicroRNA-21 (mir-21) and microRNA-143 (mir-143) have previously been identified as significan...
Guardado en:
Autores principales: | , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2011
|
Materias: | |
Acceso en línea: | https://doaj.org/article/dc0e4aba5fce45dda5061b2dcc0e226e |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:dc0e4aba5fce45dda5061b2dcc0e226e |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:dc0e4aba5fce45dda5061b2dcc0e226e2021-11-18T07:32:21ZExpression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer.1932-620310.1371/journal.pone.0028423https://doaj.org/article/dc0e4aba5fce45dda5061b2dcc0e226e2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22194833/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>MicroRNA expression is severely disrupted in carcinogenesis, however limited evidence is available validating results from cell-line models in human clinical cancer specimens. MicroRNA-21 (mir-21) and microRNA-143 (mir-143) have previously been identified as significantly deregulated in a range of cancers including cervical cancer. Our goal was to investigate the expression patterns of several well-studied microRNA species in cervical samples and compare the results to cell line samples.<h4>Methodology/principal findings</h4>We measured the expression of mir-21 and mir-143 in 142 formalin-fixed, paraffin embedded (FFPE) cervical biopsy tissue blocks, collected from Dantec Oncology Clinic, Dakar, Senegal. MicroRNA expression analysis was performed using Taqman-based real-time PCR assays. Protein immunohistochemical staining was also performed to investigate target protein expression on 72 samples. We found that mir-21 expression increased with worsening clinical diagnosis but that mir-143 was not correlated with histology. These observations were in stark contrast to previous reports involving cervical cancer cell lines in which mir-143 was consistently down-regulated but mir-21 largely unaffected. We also identified, for the first time, that cytoplasmic expression of Programmed Cell Death Protein 4 PDCD4; a known target of mir-21) was significantly lower in women with invasive cervical carcinoma (ICC) in comparison to those with cervical intraepithelial neoplasia (2-3) or carcinoma in situ (CIN2-3/CIS), although there was no significant correlation between mir-21 and PDCD4 expression, despite previous studies identifying PDCD4 transcript as a known mir-21 target.<h4>Conclusions</h4>Whilst microRNA biomarkers have a number of promising features, more studies on expression levels in histologically defined clinical specimens are required to investigate clinical relevance of discovery-based studies. Mir-21 may be of some utility in predictive screening, given that we observed a significant correlation between mir-21 expression level and worsening histological diagnosis of cervical cancer.Georgios DeftereosSimon R CorrieQinghua FengJanice MoriharaJoshua SternStephen E HawesNancy B KiviatPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 12, p e28423 (2011) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Georgios Deftereos Simon R Corrie Qinghua Feng Janice Morihara Joshua Stern Stephen E Hawes Nancy B Kiviat Expression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer. |
description |
<h4>Background</h4>MicroRNA expression is severely disrupted in carcinogenesis, however limited evidence is available validating results from cell-line models in human clinical cancer specimens. MicroRNA-21 (mir-21) and microRNA-143 (mir-143) have previously been identified as significantly deregulated in a range of cancers including cervical cancer. Our goal was to investigate the expression patterns of several well-studied microRNA species in cervical samples and compare the results to cell line samples.<h4>Methodology/principal findings</h4>We measured the expression of mir-21 and mir-143 in 142 formalin-fixed, paraffin embedded (FFPE) cervical biopsy tissue blocks, collected from Dantec Oncology Clinic, Dakar, Senegal. MicroRNA expression analysis was performed using Taqman-based real-time PCR assays. Protein immunohistochemical staining was also performed to investigate target protein expression on 72 samples. We found that mir-21 expression increased with worsening clinical diagnosis but that mir-143 was not correlated with histology. These observations were in stark contrast to previous reports involving cervical cancer cell lines in which mir-143 was consistently down-regulated but mir-21 largely unaffected. We also identified, for the first time, that cytoplasmic expression of Programmed Cell Death Protein 4 PDCD4; a known target of mir-21) was significantly lower in women with invasive cervical carcinoma (ICC) in comparison to those with cervical intraepithelial neoplasia (2-3) or carcinoma in situ (CIN2-3/CIS), although there was no significant correlation between mir-21 and PDCD4 expression, despite previous studies identifying PDCD4 transcript as a known mir-21 target.<h4>Conclusions</h4>Whilst microRNA biomarkers have a number of promising features, more studies on expression levels in histologically defined clinical specimens are required to investigate clinical relevance of discovery-based studies. Mir-21 may be of some utility in predictive screening, given that we observed a significant correlation between mir-21 expression level and worsening histological diagnosis of cervical cancer. |
format |
article |
author |
Georgios Deftereos Simon R Corrie Qinghua Feng Janice Morihara Joshua Stern Stephen E Hawes Nancy B Kiviat |
author_facet |
Georgios Deftereos Simon R Corrie Qinghua Feng Janice Morihara Joshua Stern Stephen E Hawes Nancy B Kiviat |
author_sort |
Georgios Deftereos |
title |
Expression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer. |
title_short |
Expression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer. |
title_full |
Expression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer. |
title_fullStr |
Expression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer. |
title_full_unstemmed |
Expression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer. |
title_sort |
expression of mir-21 and mir-143 in cervical specimens ranging from histologically normal through to invasive cervical cancer. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2011 |
url |
https://doaj.org/article/dc0e4aba5fce45dda5061b2dcc0e226e |
work_keys_str_mv |
AT georgiosdeftereos expressionofmir21andmir143incervicalspecimensrangingfromhistologicallynormalthroughtoinvasivecervicalcancer AT simonrcorrie expressionofmir21andmir143incervicalspecimensrangingfromhistologicallynormalthroughtoinvasivecervicalcancer AT qinghuafeng expressionofmir21andmir143incervicalspecimensrangingfromhistologicallynormalthroughtoinvasivecervicalcancer AT janicemorihara expressionofmir21andmir143incervicalspecimensrangingfromhistologicallynormalthroughtoinvasivecervicalcancer AT joshuastern expressionofmir21andmir143incervicalspecimensrangingfromhistologicallynormalthroughtoinvasivecervicalcancer AT stephenehawes expressionofmir21andmir143incervicalspecimensrangingfromhistologicallynormalthroughtoinvasivecervicalcancer AT nancybkiviat expressionofmir21andmir143incervicalspecimensrangingfromhistologicallynormalthroughtoinvasivecervicalcancer |
_version_ |
1718423317435645952 |