Abstract

AbstractThis study was undertaken to determine if advanced epithelial ovarian cancer was associated with increased serum and ascitic levels of soluble interleukin-2 receptor α (sIL-2Rα). Serum and ascitic fluid samples from 23 ovarian cancer patients were analyzed for slL-2Rα using an enzyme-linked immunosorbent assay and compared with the serum and peritoneal levels in 18 normal females. The samples were analyzed for CA-125 levels using a radioimmunoassay and the total protein was also measured. Normal individuals had low serum levels of slL-2Rα (367.5 ± 44.6 U/mL), with similar levels of slL-2Rα in the normal peritoneal fluid (438.6 ± 48.8 U/mL). In contrast, the serum and ascitic fluid levels in ovarian cancer patients were significantly higher (746.7 ± 82.9 U/mL, P = .0006; 2,656.7 ± 373.7 U/mL, P = .00002, respectively). The results for slL-2Rα were also significant when the levels were expressed per milligram of total protein. More importantly, in almost every ovarian cancer patient the ascitic slL-2Rα level far exceeded the serum level, a pattern also observed for CA-125. There was no correlation between the serum and ascitic slL-2Rα levels, or between the serum and ascitic CA-125 levels. Although the serum levels of slL-2Rα and CA-125 were elevated in the same patient, overall there was no correlation between the serum slL-2Rα and serum CA-125 levels, either when the levels were expressed in absolute units or per milligram of total protein. Similarly, there was no correlation between slL-2Rα and CA-125 levels in individual ascitic samples. While CA-125 levels may reflect an independent index of tumor burden, these results suggest that selective accumulation of slL-2Rα in the ascites may be one of the factors associated with the known nonresponsiveness of the infiltrating lymphocytes against ovarian carcinoma cells.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.