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dc.contributor.authorBromley, Michael
dc.contributor.authorRew, D
dc.contributor.authorBecciolini, Aldo
dc.contributor.authorBalzi, Manuela
dc.contributor.authorChadwick, Caroline A
dc.contributor.authorHewitt, D
dc.contributor.authorLi, Y
dc.contributor.authorPotten, Christopher S
dc.date.accessioned2010-04-01T16:25:04Z
dc.date.available2010-04-01T16:25:04Z
dc.date.issued1996
dc.identifier.citationA comparison of proliferation markers (BrdUrd, Ki-67, PCNA) determined at each cell position in the crypts of normal human colonic mucosa. 1996, 40 (2):89-100 Eur J Histochemen
dc.identifier.issn1121-760X
dc.identifier.pmid8839702
dc.identifier.urihttp://hdl.handle.net/10541/95530
dc.description.abstractSamples of microscopically normal human sigmoid colon fixed in 70% ethanol from 15 patients who had received bromodeoxyuridine (BrdUrd) prior to surgery have been reanalyzed using a combination of proliferation markers. The specimens have been immunostained for proliferating cell nuclear antigen (PCNA) and after microwave treatment, they have been stained for BrdUrd and Ki-67. The 15 patients selected comprised 5 patients whose mucosa previously gave high BrdUrd labelling indices in the crypt, 5 that gave median values for BrdUrd labelling and 5 that gave low values for bromodeoxyuridine labelling on a previous analysis using tissue fixed in 70% ethanol and formal saline and using a different antibody (Potten et al., 1992). The relative levels of labelling at each cell position in the crypts has been compared using the 3 proliferation markers with the data being compared with the BrdUrd labelling as a standard labelling for S phase cells. One objective was to see whether all three proliferation markers discriminated equally well between the three groups of patient samples. The data show that the distinction between high, medium and low values seen with BrdUrd labelling was retained when Ki-67 immunostaining was analysed. PCNA immunostaining resulted in high levels of labelling and the different levels of labelling seen with BrdUrd and Ki-67 were largely lost.
dc.language.isoenen
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshAnimals
dc.subject.meshBiological Markers
dc.subject.meshBromodeoxyuridine
dc.subject.meshCell Division
dc.subject.meshColon
dc.subject.meshHumans
dc.subject.meshImmunohistochemistry
dc.subject.meshIntestinal Mucosa
dc.subject.meshKi-67 Antigen
dc.subject.meshMiddle Aged
dc.subject.meshProliferating Cell Nuclear Antigen
dc.subject.meshRats
dc.subject.meshRats, Wistar
dc.titleA comparison of proliferation markers (BrdUrd, Ki-67, PCNA) determined at each cell position in the crypts of normal human colonic mucosa.en
dc.typeArticleen
dc.contributor.departmentCRC Department of Histology, Paterson Institute for Cancer Research, Christie Hospital (NHS) Trust, Manchester, UK.en
dc.identifier.journalEuropean Journal of Histochemistryen
html.description.abstractSamples of microscopically normal human sigmoid colon fixed in 70% ethanol from 15 patients who had received bromodeoxyuridine (BrdUrd) prior to surgery have been reanalyzed using a combination of proliferation markers. The specimens have been immunostained for proliferating cell nuclear antigen (PCNA) and after microwave treatment, they have been stained for BrdUrd and Ki-67. The 15 patients selected comprised 5 patients whose mucosa previously gave high BrdUrd labelling indices in the crypt, 5 that gave median values for BrdUrd labelling and 5 that gave low values for bromodeoxyuridine labelling on a previous analysis using tissue fixed in 70% ethanol and formal saline and using a different antibody (Potten et al., 1992). The relative levels of labelling at each cell position in the crypts has been compared using the 3 proliferation markers with the data being compared with the BrdUrd labelling as a standard labelling for S phase cells. One objective was to see whether all three proliferation markers discriminated equally well between the three groups of patient samples. The data show that the distinction between high, medium and low values seen with BrdUrd labelling was retained when Ki-67 immunostaining was analysed. PCNA immunostaining resulted in high levels of labelling and the different levels of labelling seen with BrdUrd and Ki-67 were largely lost.


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