Loss of heterozygosity at the FHIT locus is coincident with activation of DNA damage response checkpoint proteins; thus damage at fragile loci may trigger checkpoint activation. We examined preneoplastic lesions adjacent to non-small cell lung carcinomas for alterations to expression of Fhit and activated checkpoint proteins. Expression scores were analyzed for pair-wise associations and correlations among proteins and type of lesion. Hyperplastic and dysplastic lesions were positive for nuclear gamma H2AX expression; 12/20 dysplastic lesions were negative for Fhit expression. Fhit positive lesions showed expression of most checkpoint proteins examined, while Fhit negative lesions showed absence of expression of Chk1 and phosphoChk1. The results show that loss of expression of Fhit is significantly directly correlated with absence of activated Chk1 in dysplasia, and suggest a connection between loss of Fhit and modulation of checkpoint activity. (C) 2009 Elsevier Ireland Ltd. All rights reserved.

Fhit loss in lung preneoplasia: Relation to DNA damage response checkpoint activation / Cirombella, Roberto; Montrone, Giuseppe; Stoppacciaro, Antonella; Giglio, Simona; Volinia, Stefano; Graziano, Paolo; Huebner, Kay; Vecchione, Andrea. - In: CANCER LETTERS. - ISSN 0304-3835. - 291:2(2010), pp. 230-236. [10.1016/j.canlet.2009.10.017]

Fhit loss in lung preneoplasia: Relation to DNA damage response checkpoint activation

CIROMBELLA, Roberto;MONTRONE, Giuseppe;STOPPACCIARO, ANTONELLA;GIGLIO, SIMONA;Graziano, Paolo;VECCHIONE, ANDREA
2010

Abstract

Loss of heterozygosity at the FHIT locus is coincident with activation of DNA damage response checkpoint proteins; thus damage at fragile loci may trigger checkpoint activation. We examined preneoplastic lesions adjacent to non-small cell lung carcinomas for alterations to expression of Fhit and activated checkpoint proteins. Expression scores were analyzed for pair-wise associations and correlations among proteins and type of lesion. Hyperplastic and dysplastic lesions were positive for nuclear gamma H2AX expression; 12/20 dysplastic lesions were negative for Fhit expression. Fhit positive lesions showed expression of most checkpoint proteins examined, while Fhit negative lesions showed absence of expression of Chk1 and phosphoChk1. The results show that loss of expression of Fhit is significantly directly correlated with absence of activated Chk1 in dysplasia, and suggest a connection between loss of Fhit and modulation of checkpoint activity. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
2010
Chromosome fragile sites; DNA damage response checkpoint; Fhit; Preneoplastic lesions of lung; Squamous dysplasia; Acid Anhydride Hydrolases; Chromosome Fragile Sites; DNA Damage; DNA, Neoplasm; Gene Expression Regulation, Neoplastic; Heterozygote; Humans; Hyperplasia; Immunohistochemistry; In Situ Hybridization, Fluorescence; Lung Neoplasms; Neoplasm Proteins; Precancerous Conditions; Protein Kinases; Cancer Research; Oncology
01 Pubblicazione su rivista::01a Articolo in rivista
Fhit loss in lung preneoplasia: Relation to DNA damage response checkpoint activation / Cirombella, Roberto; Montrone, Giuseppe; Stoppacciaro, Antonella; Giglio, Simona; Volinia, Stefano; Graziano, Paolo; Huebner, Kay; Vecchione, Andrea. - In: CANCER LETTERS. - ISSN 0304-3835. - 291:2(2010), pp. 230-236. [10.1016/j.canlet.2009.10.017]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/869395
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