Immunohistochemical evaluation of epithelial ovarian carcinomas identifies three different expression patterns of the

Kristina Levan1,2, Matin Mehryar3, Constantina Mateoiu4

  • 1Sahlgrenska Cancer Center, Department of Obstetrics and Gynecology, Institute of Clinical Sciences, University of Gothenburg, SE-405 30, Gothenburg, Sweden. kristina.levan@gu.se.

BMC Cancer
|May 4, 2017
PubMed
Abstract

Insights

This study characterized NaPi2b expression in ovarian tumors, finding it in 93% of malignant samples. Pathological evaluation of NaPi2b may help identify patients for targeted MX35 antibody therapy.

Area of Science:

  • Oncology
  • Molecular Biology
  • Immunology

Background:

  • Ovarian cancer is often diagnosed at late stages, necessitating improved therapeutic strategies.
  • Targeting the NaPi2b membrane transporter with MX35 antibody-based therapy is a promising avenue for ovarian cancer treatment.
  • Detailed characterization of NaPi2b expression is crucial for developing effective targeted therapies.

Purpose of the Study:

  • To characterize the expression and localization of the NaPi2b transporter in ovarian tumor samples.
  • To investigate the correlation between NaPi2b expression patterns and ovarian tumor characteristics.
  • To assess the potential of NaPi2b as a target for MX35 antibody-based ovarian cancer therapy.

Main Methods:

  • Quantitative PCR (QPCR) and immunohistochemistry were used to analyze gene and protein expression of SLC34A2/NaPi2b.
  • Ovarian carcinoma tissues (n=73 for QPCR, n=136 for IHC) were examined.
  • Expression levels and antigen localization were correlated with tumor grade, histology, and clinical data.

Main Results:

  • NaPi2b protein expression was detected in 93% of malignant ovarian tumor samples.
  • Three distinct patterns of NaPi2b antigen distribution were identified within tumors.
  • Mucinous tumors showed significantly lower NaPi2b gene and protein expression compared to other types.
  • Differences in NaPi2b expression intensity and distribution were observed based on tumor grade and histology.

Conclusions:

  • NaPi2b expression levels and localization vary with ovarian tumor grade and histology.
  • Distinct NaPi2b antigen localization patterns were noted in borderline, type 1, and type 2 ovarian tumors.
  • Pathological evaluation of NaPi2b expression is recommended to guide patient selection for NaPi2b-targeted therapies, such as MX35 antibody treatment.

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