LINE-1 (L1) retrotransposons are a source of endogenous reverse transcriptase (RT) activity, which is expressed as part of the L1-encoded ORF2 protein (L1-ORF2p). L1 elements are highly expressed in many cancer types, while being silenced in most differentiated somatic tissues. We previously found that RT inhibition reduces cell proliferation and promotes differentiation in neoplastic cells, indicating that high endogenous RT activity promotes cancer growth. Here we investigate the expression of L1-ORF2p in several human types of cancer.We have developed a highly specific monoclonal antibody (mAb chA1-L1) to study ORF2p expression and localization in human cancer cells and tissues.We uncover new evidence for high levels of L1-ORF2p in transformed cell lines and staged epithelial cancer tissues (colon, prostate, lung and breast) while no or only basal ORF2p expression was detected in non-transformed cells. An in-depth analysis of colon and prostate tissues shows ORF2p expression in preneoplastic stages, namely transitional mucosa and prostate intraepithelial neoplasia (PIN), respectively.Our results show that L1-ORF2p is overexpressed in tumor and in preneoplastic colon and prostate tissues; this latter finding suggests that ORF2p could be considered as a potential early diagnostic biomarker.

De Luca, C., Guadagni, F., SINIBALDI VALLEBONA, P., Sentinelli, S., Gallucci, M., Hoffmann, A., et al. (2016). Enhanced expression of LINE-1-encoded ORF2 protein in early stages of colon and prostate transformation. ONCOTARGET, 7(4), 4048-4061 [10.18632/oncotarget.6767].

Enhanced expression of LINE-1-encoded ORF2 protein in early stages of colon and prostate transformation

SINIBALDI VALLEBONA, PAOLA;
2016-01-01

Abstract

LINE-1 (L1) retrotransposons are a source of endogenous reverse transcriptase (RT) activity, which is expressed as part of the L1-encoded ORF2 protein (L1-ORF2p). L1 elements are highly expressed in many cancer types, while being silenced in most differentiated somatic tissues. We previously found that RT inhibition reduces cell proliferation and promotes differentiation in neoplastic cells, indicating that high endogenous RT activity promotes cancer growth. Here we investigate the expression of L1-ORF2p in several human types of cancer.We have developed a highly specific monoclonal antibody (mAb chA1-L1) to study ORF2p expression and localization in human cancer cells and tissues.We uncover new evidence for high levels of L1-ORF2p in transformed cell lines and staged epithelial cancer tissues (colon, prostate, lung and breast) while no or only basal ORF2p expression was detected in non-transformed cells. An in-depth analysis of colon and prostate tissues shows ORF2p expression in preneoplastic stages, namely transitional mucosa and prostate intraepithelial neoplasia (PIN), respectively.Our results show that L1-ORF2p is overexpressed in tumor and in preneoplastic colon and prostate tissues; this latter finding suggests that ORF2p could be considered as a potential early diagnostic biomarker.
2016
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICA
English
Con Impact Factor ISI
LINE-1/L1; ORF2; retrotransposon; reverse transcriptase; tumorigenesis; Adenocarcinoma; Adenoma; Animals; Antibodies, Monoclonal; Antibody Formation; Biomarkers, Tumor; Blotting, Western; Cell Transformation, Neoplastic; Colonic Neoplasms; Deoxyribonuclease I; Endonucleases; Fluorescent Antibody Technique; Humans; Immunoenzyme Techniques; Male; Mice; Mice, Inbred BALB C; Neoplasm Grading; Neoplasm Staging; Prognosis; Prostatic Intraepithelial Neoplasia; Prostatic Neoplasms; RNA-Directed DNA Polymerase; Tissue Array Analysis; Tumor Cells, Cultured
De Luca, C., Guadagni, F., SINIBALDI VALLEBONA, P., Sentinelli, S., Gallucci, M., Hoffmann, A., et al. (2016). Enhanced expression of LINE-1-encoded ORF2 protein in early stages of colon and prostate transformation. ONCOTARGET, 7(4), 4048-4061 [10.18632/oncotarget.6767].
De Luca, C; Guadagni, F; SINIBALDI VALLEBONA, P; Sentinelli, S; Gallucci, M; Hoffmann, A; Schumann, G; Spadafora, C; Sciamanna, I
Articolo su rivista
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/173160
Citazioni
  • ???jsp.display-item.citation.pmc??? 14
  • Scopus 29
  • ???jsp.display-item.citation.isi??? 25
social impact