Cytogenetic analysis of metaplastic squamous cell carcinoma of the breast inter- and intratumoral heterogeneity

被引:3
作者
Oikawa, Masahiro [1 ,3 ,4 ]
Igawa, Akiko [1 ]
Taguchi, Kenichi [2 ]
Baba, Kimiko [1 ]
Ishida, Mayumi [1 ]
Akiyoshi, Sayuri [1 ]
Yano, Hiroshi [4 ]
Nagayasu, Takeshi [4 ]
Ohno, Shinji [5 ]
Tokunaga, Eriko [1 ]
机构
[1] Natl Kyushu Canc Ctr, Dept Breast Oncol, Minami Ku, 3-1-1 Notame, Fukuoka 8111347, Japan
[2] Natl Kyushu Canc Ctr, Dept Pathol, Fukuoka, Japan
[3] New Wa Kai Oikawa Hosp, Dept Breast Surg, Fukuoka, Japan
[4] Nagasaki Univ, Dept Surg Oncol, Grad Sch Biomed Sci, Nagasaki, Japan
[5] JFCR, Breast Oncol Ctr, Canc Inst Hosp, Tokyo, Japan
基金
日本学术振兴会;
关键词
Breast cancer; Squamous cell carcinoma; Tumor heterogeneity; Array CGH; Pathology; CANCER; EVOLUTION;
D O I
10.1007/s12282-017-0768-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Squamous cell carcinoma (SCC) of the breast is a rare and generally aggressive disease that accounts for less than 0.1% of all breast carcinomas. Although SCCs have distinct morphological features, their origin and cytogenetic profile are not well understood. Methods Five patients with SCC were studied. The tumor area that was predominantly composed of SCC components was macrodissected and DNA was extracted. In three cases, an invasive or noninvasive ductal carcinoma of no special type (NST) component was also present. NST-component DNA was also extracted. The tumor DNA was used for array comparative genomic hybridization analysis using a high-density oligonucleotide microarray. The cytogenetic profile of the SCC components was compared with each other and with the paired NST component in three of the five cases. Results The cytogenetic profile of the SCC components indicated large intertumoral heterogeneity. There were between 2 and 160 copy number alterations per case, and no common copy number alterations were identified. The cytogenetic profiles of the paired SCC and NST components were similar but not identical. Although, in one case, a larger number of copy number aberrant regions were detected in the SCC component than the NST component. In this case, all the NST component aberrations were present in the SCC component. This implies that the SCC component originated from the NST component. There were no common SCC component-specific aberrations in the three NST-component cases. Conclusion Our results demonstrate the cytogenetic interand intratumoral heterogeneity of SCC of the breast. Our comparison of cytogenetic profiles indicated that the SCC component originated from the NST component in one case.
引用
收藏
页码:733 / 741
页数:9
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