Literature DB >> 14669790

The meaning of the c-kit proto-oncogene product in malignant transformation in human mammary epithelium.

Chang Dae Ko1, Jee Soo Kim, Byung Gyun Ko, Byung Ho Son, Hee Joon Kang, Ho Sung Yoon, Eun Yoon Cho, Gyungyub Gong, Sei Hyun Ahn.   

Abstract

To evaluate the relationship between the c-kit proto-oncogene product and malignant transformation of human breast tissue, we examined the immunohistochemical expression of the c-kit proto-oncogene product in both malignant and non-malignant breast tissues. The immunohistochemical expression of the c-kit proto-oncogene product in 40 primary breast cancer tissues (22 axillary lymph nodes negative, 18 lymph nodes positive), in 18 corresponding axillary lymph nodes, and in 10 distant metastastic tissues were studied using an anti-c-kit proto-oncogene product antibody in comparison with 20 normal and 20 benign breast tissues. The mean values of immunoreactive score (IRS) were compared. The IRS of the c-kit proto-oncogene product in normal mammary epithelia was 5.90 +/- 1.37 (mean +/- s.d.). In benign tissues, the c-kit proto-oncogene product was detected heterogeneously with a reduced IRS (4.05 +/- 1.82). In primary breast cancer tissues, the expression of the c-kit proto-oncogene product was often deleted and the average IRS (0.90 +/- 1.73) was significantly reduced compared to those of the normal breast tissues or benign breast disease tissues, but no significant difference was shown between the breast cancer groups. The c-kit proto-oncogene product may correlate with growth control or the differentiation of normal breast epithelium. This result suggests that the loss of expression of this protein might correlate with malignant breast cancer progression, but it is most likely involved at an early stage of human breast cancer development.

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Year:  2003        PMID: 14669790     DOI: 10.1023/a:1027323210736

Source DB:  PubMed          Journal:  Clin Exp Metastasis        ISSN: 0262-0898            Impact factor:   5.150


  26 in total

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  18 in total

1.  Screening of the c-kit gene missense mutation in invasive ductal carcinoma of breast among north Indian population.

Authors:  Syed Rizwan Hussain; Sunil G Babu; Syed Tasleem Raza; Pradyumn Singh; Faisal Ahmed; Hena Naqvi; Farzana Mahdi
Journal:  Mol Biol Rep       Date:  2012-06-24       Impact factor: 2.316

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Journal:  Reprod Toxicol       Date:  2011-05-20       Impact factor: 3.143

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Journal:  Cell Oncol (Dordr)       Date:  2013-06-27       Impact factor: 6.730

4.  Expression and clinical significance of EGFL7 in malignant glioma.

Authors:  Chun-hai Huang; Xue-jun Li; Yi-zeng Zhou; Yong Luo; Cui Li; Xian-rui Yuan
Journal:  J Cancer Res Clin Oncol       Date:  2010-03-06       Impact factor: 4.553

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Authors:  Purevsuren Jambal; Melanie M Badtke; J Chuck Harrell; Virginia F Borges; Miriam D Post; Grace E Sollender; Monique A Spillman; Kathryn B Horwitz; Britta M Jacobsen
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Authors:  Trine Tramm; Jee-Yeon Kim; Sebastian Leibl; Farid Moinfar; Fattaneh A Tavassoli
Journal:  Virchows Arch       Date:  2016-06-10       Impact factor: 4.064

9.  Expression of c-kit proto-oncogene product in breast cancer tissues.

Authors:  Aydan Eroğlu; Aliye Sari
Journal:  Med Oncol       Date:  2007       Impact factor: 3.064

10.  Expression of c-kit protein in cancer vs. normal breast tissue.

Authors:  Abdolhassan Talaiezadeh; Seyed Nematollah Jazayeri; Jamal Nateghi
Journal:  Contemp Oncol (Pozn)       Date:  2012-09-29
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