Endometrial cancer patients have high affinity antibodies for estrogen metabolite–receptor aggregate: A potential biomarker for EC

Aim Elevated levels of 16α‐hydroxyestrone (16α‐OHE1) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial tissue, but research on their combined role is lacking. We aimed to investigate the affinity and binding specificity of EC antibodies against the 1...

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Published inThe journal of obstetrics and gynaecology research Vol. 46; no. 10; pp. 2115 - 2125
Main Authors Khan, Wahid Ali, Alsamghan, Awad Saeed, Khan, Mohd Wajid Ali
Format Journal Article
LanguageEnglish
Published Kyoto, Japan John Wiley & Sons Australia, Ltd 01.10.2020
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Abstract Aim Elevated levels of 16α‐hydroxyestrone (16α‐OHE1) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial tissue, but research on their combined role is lacking. We aimed to investigate the affinity and binding specificity of EC antibodies against the 16α‐OHE1‐ERα aggregate in the serum of EC patients. Specificities of EC antibodies were also evaluated according to various clinical characteristics found in these cancer patients. Methods The binding specificity and affinity of EC antibodies against 16α‐OHE1‐ERα in the serum of 120 EC patients were evaluated by direct binding and competition ELISA and quantitative precipitation titration. Binding of EC antibodies was also determined according to various clinical characteristics in EC patients through competition ELISA. Results Antibodies from EC patients demonstrated high recognition of 16α‐OHE1‐ERα compared to ERα (P < 0.05) or 16α‐OHE1 (P < 0.001). The relative affinity of EC IgG was 1.49 × 10−7 M, 1.34 × 10−6 M and 1.13 × 10−6 M for 16α‐OHE1‐ERα, ERα and 16α‐OHE1, respectively. Several factors, such as obesity, postmenopausal status, use of hormonal therapy, ER and progesterone receptor (PR) status, low 2‐OHE1/16α‐OHE1 ratio, chemotherapy and hypertension, augment the production of antibodies against 16α‐OHE1‐ERα in EC patients. Conclusion 16α‐OHE1‐ERα is a high‐affinity antigen for EC antibodies in the serum of EC patients and might function as a biomarker for this disease. Furthermore, several factors enhanced the production of antibodies against 16α‐OHE1‐ERα in the sera of these EC patients.
AbstractList Aim Elevated levels of 16α‐hydroxyestrone (16α‐OHE1) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial tissue, but research on their combined role is lacking. We aimed to investigate the affinity and binding specificity of EC antibodies against the 16α‐OHE1‐ERα aggregate in the serum of EC patients. Specificities of EC antibodies were also evaluated according to various clinical characteristics found in these cancer patients. Methods The binding specificity and affinity of EC antibodies against 16α‐OHE1‐ERα in the serum of 120 EC patients were evaluated by direct binding and competition ELISA and quantitative precipitation titration. Binding of EC antibodies was also determined according to various clinical characteristics in EC patients through competition ELISA. Results Antibodies from EC patients demonstrated high recognition of 16α‐OHE1‐ERα compared to ERα (P < 0.05) or 16α‐OHE1 (P < 0.001). The relative affinity of EC IgG was 1.49 × 10−7 M, 1.34 × 10−6 M and 1.13 × 10−6 M for 16α‐OHE1‐ERα, ERα and 16α‐OHE1, respectively. Several factors, such as obesity, postmenopausal status, use of hormonal therapy, ER and progesterone receptor (PR) status, low 2‐OHE1/16α‐OHE1 ratio, chemotherapy and hypertension, augment the production of antibodies against 16α‐OHE1‐ERα in EC patients. Conclusion 16α‐OHE1‐ERα is a high‐affinity antigen for EC antibodies in the serum of EC patients and might function as a biomarker for this disease. Furthermore, several factors enhanced the production of antibodies against 16α‐OHE1‐ERα in the sera of these EC patients.
AimElevated levels of 16α‐hydroxyestrone (16α‐OHE1) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial tissue, but research on their combined role is lacking. We aimed to investigate the affinity and binding specificity of EC antibodies against the 16α‐OHE1‐ERα aggregate in the serum of EC patients. Specificities of EC antibodies were also evaluated according to various clinical characteristics found in these cancer patients.MethodsThe binding specificity and affinity of EC antibodies against 16α‐OHE1‐ERα in the serum of 120 EC patients were evaluated by direct binding and competition ELISA and quantitative precipitation titration. Binding of EC antibodies was also determined according to various clinical characteristics in EC patients through competition ELISA.ResultsAntibodies from EC patients demonstrated high recognition of 16α‐OHE1‐ERα compared to ERα (P < 0.05) or 16α‐OHE1 (P < 0.001). The relative affinity of EC IgG was 1.49 × 10−7 M, 1.34 × 10−6 M and 1.13 × 10−6 M for 16α‐OHE1‐ERα, ERα and 16α‐OHE1, respectively. Several factors, such as obesity, postmenopausal status, use of hormonal therapy, ER and progesterone receptor (PR) status, low 2‐OHE1/16α‐OHE1 ratio, chemotherapy and hypertension, augment the production of antibodies against 16α‐OHE1‐ERα in EC patients.Conclusion16α‐OHE1‐ERα is a high‐affinity antigen for EC antibodies in the serum of EC patients and might function as a biomarker for this disease. Furthermore, several factors enhanced the production of antibodies against 16α‐OHE1‐ERα in the sera of these EC patients.
Abstract Aim Elevated levels of 16α‐hydroxyestrone (16α‐OHE 1 ) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial tissue, but research on their combined role is lacking. We aimed to investigate the affinity and binding specificity of EC antibodies against the 16α‐OHE 1 ‐ERα aggregate in the serum of EC patients. Specificities of EC antibodies were also evaluated according to various clinical characteristics found in these cancer patients. Methods The binding specificity and affinity of EC antibodies against 16α‐OHE 1 ‐ERα in the serum of 120 EC patients were evaluated by direct binding and competition ELISA and quantitative precipitation titration. Binding of EC antibodies was also determined according to various clinical characteristics in EC patients through competition ELISA. Results Antibodies from EC patients demonstrated high recognition of 16α‐OHE 1 ‐ERα compared to ERα ( P  < 0.05) or 16α‐OHE 1 ( P  < 0.001). The relative affinity of EC IgG was 1.49 × 10 −7  M, 1.34 × 10 −6  M and 1.13 × 10 −6  M for 16α‐OHE 1 ‐ERα, ERα and 16α‐OHE 1 , respectively. Several factors, such as obesity, postmenopausal status, use of hormonal therapy, ER and progesterone receptor (PR) status, low 2‐OHE 1 /16α‐OHE 1 ratio, chemotherapy and hypertension, augment the production of antibodies against 16α‐OHE 1 ‐ERα in EC patients. Conclusion 16α‐OHE 1 ‐ERα is a high‐affinity antigen for EC antibodies in the serum of EC patients and might function as a biomarker for this disease. Furthermore, several factors enhanced the production of antibodies against 16α‐OHE 1 ‐ERα in the sera of these EC patients.
AIMElevated levels of 16α-hydroxyestrone (16α-OHE1 ) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial tissue, but research on their combined role is lacking. We aimed to investigate the affinity and binding specificity of EC antibodies against the 16α-OHE1 -ERα aggregate in the serum of EC patients. Specificities of EC antibodies were also evaluated according to various clinical characteristics found in these cancer patients. METHODSThe binding specificity and affinity of EC antibodies against 16α-OHE1 -ERα in the serum of 120 EC patients were evaluated by direct binding and competition ELISA and quantitative precipitation titration. Binding of EC antibodies was also determined according to various clinical characteristics in EC patients through competition ELISA. RESULTSAntibodies from EC patients demonstrated high recognition of 16α-OHE1 -ERα compared to ERα (P < 0.05) or 16α-OHE1 (P < 0.001). The relative affinity of EC IgG was 1.49 × 10-7  M, 1.34 × 10-6  M and 1.13 × 10-6  M for 16α-OHE1 -ERα, ERα and 16α-OHE1 , respectively. Several factors, such as obesity, postmenopausal status, use of hormonal therapy, ER and progesterone receptor (PR) status, low 2-OHE1 /16α-OHE1 ratio, chemotherapy and hypertension, augment the production of antibodies against 16α-OHE1 -ERα in EC patients. CONCLUSION16α-OHE1 -ERα is a high-affinity antigen for EC antibodies in the serum of EC patients and might function as a biomarker for this disease. Furthermore, several factors enhanced the production of antibodies against 16α-OHE1 -ERα in the sera of these EC patients.
Author Khan, Mohd Wajid Ali
Khan, Wahid Ali
Alsamghan, Awad Saeed
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CitedBy_id crossref_primary_10_1080_01635581_2022_2123535
crossref_primary_10_1080_1354750X_2023_2179114
crossref_primary_10_1155_2022_9304392
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Snippet Aim Elevated levels of 16α‐hydroxyestrone (16α‐OHE1) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial...
Abstract Aim Elevated levels of 16α‐hydroxyestrone (16α‐OHE 1 ) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in...
AimElevated levels of 16α‐hydroxyestrone (16α‐OHE1) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial tissue,...
AIMElevated levels of 16α-hydroxyestrone (16α-OHE1 ) have been described in endometrial cancer (EC) and estrogen receptors (ER) expressed in endometrial...
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wiley
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StartPage 2115
SubjectTerms 16α‐hydroxyestrone
Affinity
Antibodies
Biomarkers
Cancer
Chemotherapy
Competition
ELISA
Endometrial cancer
Endometrium
estrogen receptor
Estrogen receptors
Immunoglobulin G
Metabolites
Post-menopause
Progesterone
Titration
Title Endometrial cancer patients have high affinity antibodies for estrogen metabolite–receptor aggregate: A potential biomarker for EC
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjog.14413
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