Article Data

  • Views 273
  • Dowloads 112

Original Research

Open Access

Clinical significance of serum growth-regulated oncogene α (GROα) in patients with gynecological cancer

  • R. Nishikawa1
  • 'N. Suzumori1,*,
  • T. Nishiyama2
  • H. Nishikawa1
  • A. Arakawa1
  • M. Sugiura-Ogasawara1

1Department of Obstetrics and Gynecology, Nagoya City University, Graduate School of Medicine, Nagoya, Japan

2Clinical Research Management Center, Nagoya City University, Nagoya, Japan

DOI: 10.12892/ejgo201202138 Vol.33,Issue 2,March 2012 pp.138-141

Published: 10 March 2012

*Corresponding Author(s): 'N. Suzumori E-mail: og.n.suz@med.nagoya-cu.ac.jp

Abstract

Purpose of investigation: To assess the clinical relevance of serum growth-regulated oncogene alpha (GRO alpha) levels in gynecological cancer, we investigated its concentration in distinguishing patients with cervical cancer, endometrial cancer, ovarian cancer, benign ovarian tumor and control. Methods: Preoperative serum GRO alpha levels were measured in women with cervical cancer (n = 46), endometrial cancer (n = 39), ovarian cancer (n = 124), benign ovarian tumors (n = 52), and normal controls (n = 38) using an enzyme-linked immunosorbent assay. Results: Statistical analyses showed that the serum GRO alpha concentration was significantly elevated in the cervical cancer, endometrial cancer and ovarian cancer patients compared with controls. Using GRO alpha levels, the receiver operating characteristic (ROC) of cervical cancer (AUG approximate to 0.775), endometrial cancer (AUG approximate to 0.799), ovarian cancer (AUC approximate to 0.749) and benign ovarian tumors (AUC approximate to 0.568) vs controls were identified. Conclusion: Our findings suggest that serum GRO alpha measurement as a molecular marker might contribute to detection and diagnosis of gynecological cancer.

Keywords

Cancer; GRO; ELISA; Ovarian tumor; Serum; ROC

Cite and Share

R. Nishikawa,'N. Suzumori,T. Nishiyama,H. Nishikawa,A. Arakawa,M. Sugiura-Ogasawara. Clinical significance of serum growth-regulated oncogene α (GROα) in patients with gynecological cancer. European Journal of Gynaecological Oncology. 2012. 33(2);138-141.

References

[1] Strieter R.M., Belperio J.A., Phillips R.J., Keane M.P.: “CXC chemokines in angiogenesis of cancer”. Semin. Cancer Biol., 2004, 14, 195.

[2] Kulbe H., Levinson N.R., Balkwill F., Wilson J.L.: “The chemokine network in cancer-much more than directing cell movement”. Int. J. Dev. Biol., 2004, 48, 489.

[3] Anisowicz A., Bardwell L., Sager R.: “Constitutive overexpression of a growth-regulated gene in transformed Chinese hamster and human cells”. Proc. Natl. Acad. Sci USA, 1987, 84, 7188.

[4] Richmond A., Thomas H.G.: “Melanoma growth: isolation from human melanoma tumors and characterization of tissue distribution”. J. Cell. Biochem., 1988, 36, 185.

[5] Shattuck R.L., Wood L.D., Jaffe G.J., Richmond A.: “MGSA/GRO transcription is differentially regulated in normal retinal pigment epithelial and melanoma cells”. Mol. Cell. Biol., 1994, 14, 791.

[6] Dong G., Loukinova E., Chen Z., Gangi L., Chanturita T.I., Liu E.T., Van Waes G.: “Molecular profiling of transformed and metastatic murine squamous carcinoma cells by differential display and cDNA microarray reveals altered expression of multiple genes related to growth, apoptosis, angiogenesis, and the NFB signal pathway”. Cancer Res., 2001, 61, 4797.

[7] Loukinova E., Dong G., Enamorado-Ayala I., Thomas G.R., Chen Z., Schreiber H., Van Waes C.: “Growth regulated oncogeneexpression by murine squamous cell carcinoma promotes tumor growth, metastasis, leukocyte infiltration and angiogenesis by a host CXC receptor-2 dependent mechanism”. Oncogene, 2000, 19, 3477.

[8] Li A., Varney M.L., Singh R.K.: “Constitutive expression of growth regulated oncogene (gro) in human colon carcinoma cells with different metastatic potential and its role in regulating their metastatic phenotype”. Clin. Exp. Metastasis, 2004, 21, 571.

[9] Eck M., Schmausser B., Scheller K., Brandlein S., Muller-Hermelink H.K.: “Pleiotropic effects of CXC chemokines in gastric carcinoma: differences in CXCL8 and CXCL1 expression between diffuse and intestinal types of gastric carcinoma”. Clin. Exp. Immunol., 2003, 134, 508.

[10] Shintani S., Ishikawa T., Nonaka T., Li C., Nakashiro K., Wong D.T., Hamakawa H.: “Growth-regulated oncogene-1 expression is associated with angiogenesis and lymph node metastasis in human oral cancer”. Oncology, 2004, 66, 316.

[11] Lee Z., Swaby R.F., Liang Y., Yu S., Liu S., Lu K.H. et al.: “Lysophosphatidic acid is a major regulator of growth-regulated oncogene alpha in ovarian cancer”. Cancer Res., 2006, 66, 2740.

[12] Lambeck A.J.A., Crijns A.P.G., Leffers N., Sluiter W.J., ten Hoor K.A., Braid M. et al.: “Serum cytokine profiling as a diagnostic and prognostic tool in ovarian cancer: a potential role for interleukin 7”. Clin. Cancer Res., 2007, 13, 2385.

[13] Wilson J., Balkwill F.: “The role of cytokines in the epithelial cancer microenvironment”. Semin. Cancer Biol., 2002, 12, 113.

[14] Balkwill F., Mantovani A.: “Inflammation and cancer: back to Virchow?”. Lancet, 2001, 357, 539.

[15] Vicari A.P., Caux C.: “Chemokines in cancer”. Cytokine Growth Factor Rev., 2002, 13, 143.

[16] Yang G., Rosen D.G., Zhang Z., Bast Jr R.C., Mills G.B., Colacino J.A. et al.: “The chomokine growth-regulated oncogne 1 (Gro-1) links RAS signaling to the senescence of stromal fibroblasts and ovarian tumorigenesis”. Proc. Natl. Acad. Sci USA, 2006, 103, 16472.

[17] Coffman R.L., von der Weid T.: “Multiple pathways for the initiation of T helper 2 (Th2) responses”. J. Exp. Med., 1997, 185, 373.

[18] Niwa Y.: “Elevated RANTES levels in plasma or skin and decreased plasma IL-10 levels in subsets of patients with severe atopic dermatitis”. Arch. Dermatol., 2000, 136, 125.

[19] R Development Core Team. R: “A language and environment for statistical computing”. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0. 2009.

[20] DeLong E.R., DeLong D.M., D.L. Clarke-Pearson: “Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach”. Biometrics, 1988, 44, 837.

[21] Gorelik E., Landsittel D.P., Marrangoni A.M., Modugno F., Velikokhatnaya L., Winans M.T. et al.: “Multiplexed immunobeadbased cytokine profiling for early detection of ovarian cancer”. Cancer Epidemiol Biomarkers Prev., 2005, 14, 981.

[22] Cooper B.C., Ritchie J.M., Broghammer C.L.W., Coffin J., Sorosky J.I., Buller R.E. et al.: “Preoperative serum vascular endothelial growth factor levels: significance in ovarian cancer”. Clin. Cancer Res., 2002, 8, 3193.

[23] Bast R.C. Jr, Xu F.J., Yu Y.H., Barnhill S., Zhang Z., Mills G.B.: “CA125: the past and the future”. Int. J. Biol. Markers, 1998, 13, 179.

[24] Nosov V., Su F., Amneus M., Birrer M., Robins T., Kotlerman J. et al.: “Validation of serum biomarker for detection of early-stage ovarian cancer”. Am. J. Obstet. Gynecol., 2009, 200, 639.e1.

[25] Moore R.G., Brown A.K., Miller M.C., Badgwell D., Lu Z., Allard W.J. et al.: “Utility of a novel serum biomarker HE4 in patients with endometrioid adenocarcinoma of the uterus”. Gynecol. Oncol., 2008, 110, 196.

[26] Ahuja S.K., Phillip M.M.: “The CXC chemokines growth-regulated oncogene (GRO)α, GROβ, GROγ, neutrophil-activating peptide-2, and epithelial cell-derived neutrophil-activating peptide-78 are potent agonists for the type B, but not the type A, human interleukin-8 receptor”. J. Biol. Chem., 1996, 271, 20545.

[27] Yang G., Rosen D.G., Liu G., Yang F., Guo X., Xiao X. et al.: “CXCR2 promotes ovarian cancer growth through dysregulated cell cycle, diminished apoptosis, and enhanced angiogenesis”. Clin. Caner Res., 2010, 16, 3875.

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