» Articles » PMID: 15014034

Elevated Serum Insulin-like Growth Factor Binding Protein-2 As a Prognostic Marker in Patients with Ovarian Cancer

Overview
Journal Clin Cancer Res
Specialty Oncology
Date 2004 Mar 12
PMID 15014034
Citations 46
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: The purpose of this research was to examine the diagnostic and prognostic significance of elevated serum insulin-like growth factor binding protein (IGFBP)-2 levels in women with ovarian cancer from diagnosis through treatment to relapse or remission.

Experimental Design: Serum collected pre- and postoperatively in women newly diagnosed with ovarian cancer, during adjuvant chemotherapy cycles, at 6 months follow-up and at relapse was analyzed for IGFBP-2. Control serum was from women undergoing pelvic or abdominal surgery for benign ovarian disease or nonovarian pathology.

Results: IGFBP-2 at diagnosis was significantly elevated (P < 0.0001) in women with ovarian cancer (887 +/- 62 ng/ml) compared with benign controls (337 +/- 25 ng/ml), and women undergoing nonovarian surgery (439 +/- 49 ng/ml) and correlated positively with tumor stage and cellular differentiation but not with CA125. Unexpectedly, IGFBP-2 levels increased additionally 1-week postoperatively in ovarian cancer patients (1581 +/- 90 ng/ml; P = 0.0027) as well as controls (977 +/- 95 ng/ml; P < 0.0001) and was higher in women who had suboptimal debulking compared with optimal debulking of their tumor. IGFBP-2 levels returned to normal in women without evidence of progressive disease, but remained significantly elevated in women who later relapsed. Patients with IGFBP-2 levels in the highest tertile at diagnosis had a significantly shorter progression-free interval and overall survival.

Conclusion: In ovarian cancer IGFBP-2 is elevated at diagnosis, and corresponds to stage and histology with patients in the highest tertile of IGFBP-2 more likely to relapse and have a poorer outlook. Identification of these patients at diagnosis may allow more individualized, aggressive adjuvant treatment and follow-up, and IGFBP-2 may therefore be an important additional prognostic marker in this disease.

Citing Articles

Losartan rewires the tumor-immune microenvironment and suppresses IGF-1 to overcome resistance to chemo-immunotherapy in ovarian cancer.

Sun Y, Yin Z, Li S, Wu L, Zhang Y, Zhao Y Br J Cancer. 2024; 131(10):1683-1693.

PMID: 39369055 PMC: 11554678. DOI: 10.1038/s41416-024-02863-9.


The IGF-PAPP-A-Stanniocalcin Axis in Serum and Ascites Associates with Prognosis in Patients with Ovarian Cancer.

Hjortebjerg R, Hogdall C, Hansen K, Hogdall E, Frystyk J Int J Mol Sci. 2024; 25(4).

PMID: 38396692 PMC: 10888379. DOI: 10.3390/ijms25042014.


IGFBP2 promotes proliferation and cell migration through STAT3 signaling in Sonic hedgehog medulloblastoma.

Kunhiraman H, McSwain L, Shahab S, Gershon T, MacDonald T, Kenney A Acta Neuropathol Commun. 2023; 11(1):62.

PMID: 37029430 PMC: 10082504. DOI: 10.1186/s40478-023-01557-2.


The "Sweet Spot" of Targeting Tumor Metabolism in Ovarian Cancers.

Tondo-Steele K, McLean K Cancers (Basel). 2022; 14(19).

PMID: 36230617 PMC: 9562887. DOI: 10.3390/cancers14194696.


Gold Nanoparticles Disrupt the IGFBP2/mTOR/PTEN Axis to Inhibit Ovarian Cancer Growth.

Hossen M, Wang L, Dwivedi S, Zhang Y, Rao G, Elechalwar C Adv Sci (Weinh). 2022; 9(31):e2200491.

PMID: 36104215 PMC: 9631030. DOI: 10.1002/advs.202200491.