Article Data

  • Views 653
  • Dowloads 147

Original Research

Open Access

Immunohistochemical analysis of IQGAP2 in ovarian cancer

  • Xiang Wang1,2
  • Zhuo Deng3
  • Lijie Wang1,2
  • He Chen1,2
  • Huilian Hou4
  • Xu Li1,2,*,

1Center for Translational Medicine, the First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, China

2Key Laboratory for Tumor Precision Medicine of Shaanxi Province, the First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, China

3Department of Obstetrics and Gynecology, Shaanxi Provincial People’s Hospital, Xi’an, China

4Department of Pathology, the First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, China

DOI: 10.12892/ejgo4408.2019 Vol.40,Issue 1,February 2019 pp.74-79

Accepted: 26 September 2017

Published: 10 February 2019

*Corresponding Author(s): Xu Li E-mail: lixu56@mail.xjtu.edu.cn

Abstract

IQ motif-containing GTPase-activating protein 2 (IQGAP2) was regarded as a tumor suppressor in some cancers, but its expression pattern in various histological subtypes of ovarian cancer has not been investigated. Immunohistochemical staining for IQGAP2 was conducted with two human ovarian tissue microarrays containing 250 ovarian tumors and 39 normal ovarian tissues in total. Positive staining of IQGAP2 was observed in cytoplasm as well as on membrane. IQGAP2 was expressed in 48.7% of normal ovarian tissues, 37.9% of serous cancers, 66.7% of mucinous cancer, 71.4% of endometrioid cancers, 100% of clear cell cancers, 25% of endodermal sinus tumors, and immature teratomas. Contrarily, IQGAP2 was absent in dysgerminomas, transitional, and granulosa cell tumors. The mean IQGAP2 immunohistochemical composite scores were 1.92 for normal ovarian tissues,1.69 for serous cancers, 4.51 for mucinous cancers, 3.00 for endometrioid cancers, 7.71 for clear cell cancers, 0.25 for endodermal sinus tumors, and 1 for immature teratomas. Compared with normal ovarian tissues, the overall positivity of IQGAP2 in clear cell cancers and the mean composite scores of IQGAP2 in clear cell and mucinous cancers were significantly higher, while the mean composite scores of IQGAP2 in dysgerminomas, endodermal sinus tumor, and granulosa cell tumors was significantly lower. The authors concluded that IQGAP2 might serve as a tumor suppressor in dysgerminomas, endodermal sinus tumor, and granulosa cell tumors of ovary. Understanding the role of IQGAP2 in the pathogenesis of ovarian cancers necessitates further study.

Keywords

Ovarian cancer; Immunohistochemistry; IQGAP2

Cite and Share

Xiang Wang,Zhuo Deng,Lijie Wang,He Chen,Huilian Hou,Xu Li. Immunohistochemical analysis of IQGAP2 in ovarian cancer. European Journal of Gynaecological Oncology. 2019. 40(1);74-79.

References

[1] Ferlay J., Soerjomataram I., Dikshit R., Eser S., Mathers C., Rebelo M., et al.: “Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012”. Int. J. Cancer, 2015, 136(5),E359-386.

[2] Agarwal R.,Kaye S.B.: “Ovarian cancer: strategies for overcoming resistance to chemotherapy”. Nat Rev Cancer, 2003, 3, 502.

[3] Hedman A.C., Smith J.M.,Sacks D.B.: “The biology of IQGAP proteins: beyond the cytoskeleton”. EMBO Rep., 2015, 16, 427.

[4] Briggs M.W.,Sacks D.B.: “IQGAP proteins are integral components of cytoskeletal regulation”. EMBO Rep., 2003, 4, 571.

[5] White C.D., Brown M.D.,Sacks D.B.: “IQGAPs in cancer: a family of scaffold proteins underlying tumorigenesis”. FEBS Lett., 2009, 583, 1817.

[6] White C.D., Erdemir H.H.,Sacks D.B.: “IQGAP1 and its binding proteins control diverse biological functions”. Cell Signal., 2012, 24, 826.

[7] Smith J.M., Hedman A.C.,Sacks D.B.: “IQGAPs choreograph cellular signaling from the membrane to the nucleus”. Trends Cell. Biol., 2015, 25, 171.

[8] Mataraza J.M., Briggs M.W., Li Z., Entwistle A., Ridley A.J.,Sacks D.B.: “IQGAP1 promotes cell motility and invasion”. J. Biol. Chem., 2003, 278, 41237.

[9] Nabeshima K., Shimao Y., Inoue T.,Koono M.: “Immunohistochemical analysis of IQGAP1 expression in human colorectal carcinomas: its overexpression in carcinomas and association with invasion fronts”. Cancer Lett., 2002, 176, 101.

[10] White C.D., Khurana H., Gnatenko D.V., Li Z., Odze R.D., Sacks D.B., et al.: “IQGAP1 and IQGAP2 are reciprocally altered in hepatocellular carcinoma”. BMC Gastroenterol., 2010, 10, 125.

[11] Xia F.D., Wang Z.L., Chen H.X., Huang Y., Li J.D., Wang Z.M., et al.: “Differential expression of IQGAP1/2 in Hepatocellular carcinoma and its relationship with clinical outcomes”. Asian Pac. J. Cancer Prev., 2014, 15, 4951.

[12] Gnatenko D.V., Xu X., Zhu W.,Schmidt V.A.: “Transcript profiling identifies iqgap2(-/-) mouse as a model for advanced human hepatocellular carcinoma”. PLoS One, 2013, 8, e71826.

[13] Schmidt V.A., Chiariello C.S., Capilla E., Miller F.,Bahou W.F.: “Development of hepatocellular carcinoma in Iqgap2-deficient mice is IQGAP1 dependent”. Mol. Cell Biol., 2008, 28, 1489.

[14] Jin S.H., Akiyama Y., Fukamachi H., Yanagihara K., Akashi T.,Yuasa Y.: “IQGAP2 inactivation through aberrant promoter methylation and promotion of invasion in gastric cancer cells”. Int. J. Cancer, 2008, 122, 1040.

[15] Xie Y., Yan J., Cutz J.C., Rybak A.P., He L., Wei F., et al.: “IQGAP2, A candidate tumour suppressor of prostate tumorigenesis”. Biochim. Biophys. Acta, 2012, 1822, 875.

[16] Zhou R., Guo Z., Watson C., Chen E., Kong R., Wang W., et al.: “Polarized distribution of IQGAP proteins in gastric parietal cells and their roles in regulated epithelial cell secretion”. Mol. Biol. Cell, 2003, 14, 1097.

[17] Yamashiro S., Noguchi T.,Mabuchi I.: “Localization of two IQGAPs in cultured cells and early embryos of Xenopus laevis”. Cell. Motil. Cytoskeleton, 2003, 55, 36.

[18] Tewari K., Cappuccini F., Disaia P.J., Berman M.L., Manetta A.,Kohler M.F.: “Malignant germ cell tumors of the ovary”. Obstet. Gynecol., 2000, 95,128-133.

[19] Pectasides D., Pectasides E.,Kassanos D.: “Germ cell tumors of the ovary”. Cancer Treat. Rev., 2008, 34, 427.

[20] Colombo N., Parma G., Zanagnolo V.,Insinga A.: “Management of ovarian stromal cell tumors”. J. Clin. Oncol., 2007, 25, 2944.

[21] Schumer S.T.,Cannistra S.A.: “Granulosa cell tumor of the ovary”. J. Clin. Oncol., 2003, 21, 1180.

Abstracted / indexed in

Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,500 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.

Biological Abstracts Easily discover critical journal coverage of the life sciences with Biological Abstracts, produced by the Web of Science Group, with topics ranging from botany to microbiology to pharmacology. Including BIOSIS indexing and MeSH terms, specialized indexing in Biological Abstracts helps you to discover more accurate, context-sensitive results.

Google Scholar Google Scholar is a freely accessible web search engine that indexes the full text or metadata of scholarly literature across an array of publishing formats and disciplines.

JournalSeek Genamics JournalSeek is the largest completely categorized database of freely available journal information available on the internet. The database presently contains 39226 titles. Journal information includes the description (aims and scope), journal abbreviation, journal homepage link, subject category and ISSN.

Current Contents - Clinical Medicine Current Contents - Clinical Medicine provides easy access to complete tables of contents, abstracts, bibliographic information and all other significant items in recently published issues from over 1,000 leading journals in clinical medicine.

BIOSIS Previews BIOSIS Previews is an English-language, bibliographic database service, with abstracts and citation indexing. It is part of Clarivate Analytics Web of Science suite. BIOSIS Previews indexes data from 1926 to the present.

Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.

Submission Turnaround Time

Conferences

Top