Detection of MCM5 as a novel non-invasive aid for the diagnosis of endometrial and ovarian tumours.
Biomarker
Early detection
Endometrial cancer
MCM5
Ovarian cancer
Journal
BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800
Informations de publication
Date de publication:
15 Oct 2020
15 Oct 2020
Historique:
received:
02
05
2020
accepted:
28
09
2020
entrez:
16
10
2020
pubmed:
17
10
2020
medline:
23
4
2021
Statut:
epublish
Résumé
MCM5 is a protein involved in DNA replication, facilitating cell proliferation. In normal epithelium MCM5 expression is restricted to the cells in the basal proliferative compartments, however in the presence of a tumour MCM5 positive cells are present at the surface epithelium and are shed into bodily fluids. The aim of this study was to determine the sensitivity of MCM5 as a biomarker for the detection of endometrial and ovarian cancer. Patients with known ovarian or endometrial cancers, or known benign gynaecological conditions, were enrolled. Informed consent was obtained prior to the collection of full void urine, and either a vaginal tampon (worn for 6-8 h), or a vaginal swab. Vaginal secretions were extracted from the tampon or swab, centrifuged and lysed. Urine samples were centrifuged and lysed. MCM5 levels were determined by MCM5-ELISA (Arquer Diagnostics Ltd). 125 patients completed the study protocol, 41 patients had endometrial cancer, 26 ovarian cancer, and 58 benign controls. All patients provided a urine sample and either a tampon or vaginal swab sample. Urine MCM5 levels were higher in cancer patients than controls (p < 0.0001), there was no significant difference in levels between tampon samples or vaginal swab samples in cancer patients when compared to controls. Performance of MCM5 to discriminate cancer from benign disease was high with an area under the ROC curve of 0.83 for endometrial cancer and 0.68 for ovarian cancer. Using a cut off of 12 pg/mL, overall sensitivity for endometrial cancer was 87.8, and 61.5% for ovarian cancer with a specificity of 75.9%. MCM5 is a novel sensitive and specific biomarker for the detection of ovarian and endometrial tumours in urine samples, which is likely to have clinical utility as a diagnostic aid.
Sections du résumé
BACKGROUND
BACKGROUND
MCM5 is a protein involved in DNA replication, facilitating cell proliferation. In normal epithelium MCM5 expression is restricted to the cells in the basal proliferative compartments, however in the presence of a tumour MCM5 positive cells are present at the surface epithelium and are shed into bodily fluids. The aim of this study was to determine the sensitivity of MCM5 as a biomarker for the detection of endometrial and ovarian cancer.
METHODS
METHODS
Patients with known ovarian or endometrial cancers, or known benign gynaecological conditions, were enrolled. Informed consent was obtained prior to the collection of full void urine, and either a vaginal tampon (worn for 6-8 h), or a vaginal swab. Vaginal secretions were extracted from the tampon or swab, centrifuged and lysed. Urine samples were centrifuged and lysed. MCM5 levels were determined by MCM5-ELISA (Arquer Diagnostics Ltd).
RESULTS
RESULTS
125 patients completed the study protocol, 41 patients had endometrial cancer, 26 ovarian cancer, and 58 benign controls. All patients provided a urine sample and either a tampon or vaginal swab sample. Urine MCM5 levels were higher in cancer patients than controls (p < 0.0001), there was no significant difference in levels between tampon samples or vaginal swab samples in cancer patients when compared to controls. Performance of MCM5 to discriminate cancer from benign disease was high with an area under the ROC curve of 0.83 for endometrial cancer and 0.68 for ovarian cancer. Using a cut off of 12 pg/mL, overall sensitivity for endometrial cancer was 87.8, and 61.5% for ovarian cancer with a specificity of 75.9%.
CONCLUSIONS
CONCLUSIONS
MCM5 is a novel sensitive and specific biomarker for the detection of ovarian and endometrial tumours in urine samples, which is likely to have clinical utility as a diagnostic aid.
Identifiants
pubmed: 33059604
doi: 10.1186/s12885-020-07468-y
pii: 10.1186/s12885-020-07468-y
pmc: PMC7559715
doi:
Substances chimiques
Biomarkers, Tumor
0
Cell Cycle Proteins
0
MCM5 protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1000Subventions
Organisme : Arquer Diagnostics Ltd
ID : n/a
Références
J Clin Pathol. 2005 May;58(5):525-34
pubmed: 15858126
Lancet. 2016 Mar 12;387(10023):1094-1108
pubmed: 26354523
Lancet. 2016 Mar 5;387(10022):945-956
pubmed: 26707054
Lancet. 2019 Mar 23;393(10177):1240-1253
pubmed: 30910306
Br J Cancer. 2010 Aug 24;103(5):701-7
pubmed: 20648010
Cancer Epidemiol Biomarkers Prev. 2004 May;13(5):882-8
pubmed: 15159323
Gynecol Oncol. 2015 Apr;137(1):14-22
pubmed: 25677060
Clin Chem. 2016 May;62(5):737-42
pubmed: 27001493
Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14539-44
pubmed: 16199513
Sci Transl Med. 2013 Jan 9;5(167):167ra4
pubmed: 23303603
J Proteome Res. 2013 Dec 6;12(12):5383-94
pubmed: 24063748
Eur Urol Oncol. 2020 Feb;3(1):42-46
pubmed: 31307961
BMJ. 2015 Oct 28;351:h5527
pubmed: 26511519