COMPARATIVE STUDY
JOURNAL ARTICLE
Add like
Add dislike
Add to saved papers

Expression of monoclonal antibody-defined tumor markers in four carcinomas.

The specificity of monoclonal antibody-based, CA 125, CA 15-3, CA 19-9 and carcinoembryonic antigen (CEA) immunoassays were evaluated by studying how these tumor markers are expressed, using serial serum specimens from patients with breast, ovarian, colorectal, and pancreatic carcinomas. It was found that none of the monoclonal defined markers was specific for any single malignant disease. Multiple markers of increased concentration were found in all serial specimens. However, only one dominant marker was associated with each type of malignant disease. Taking advantage of the different patterns of these tumor markers expressed among different carcinomas, it was demonstrated that the specificity of these monoclonal immunoassays for diagnosis and screening of cancers could be improved if ratios of the dominant marker to other markers were determined. For example, determining ratios of CA 15-3/CEA, CA 15-3/CA 125, and CA 15-3/CA 19-9 will improve the differentiation of elevated CA 15-3 of breast carcinoma from those of colon, ovarian, and pancreatic carcinomas, respectively.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app