Comparative Genomic Hybridization Array Analysis and Real-Time PCR Reveals Genomic Copy Number Alteration for Lung Adenocarcinomas

Lung ◽  
2006 ◽  
Vol 184 (6) ◽  
pp. 355-362 ◽  
Author(s):  
Jin Soo Choi ◽  
Long Tai Zheng ◽  
Eunyoung Ha ◽  
Yun Jeong Lim ◽  
Yeul Hong Kim ◽  
...  
2006 ◽  
Vol 97 (8) ◽  
pp. 746-752 ◽  
Author(s):  
Hiroaki Kawanishi ◽  
Takeshi Takahashi ◽  
Masaaki Ito ◽  
Jun Watanabe ◽  
Shin Higashi ◽  
...  

2006 ◽  
Vol 175 (4S) ◽  
pp. 198-199
Author(s):  
Takeshi Takahashi ◽  
Hiroaki Kawanishi ◽  
Masaaki Ito ◽  
Jun Watanabe ◽  
Shin Higashi ◽  
...  

2010 ◽  
Vol 134 (7) ◽  
pp. 1063-1069 ◽  
Author(s):  
Joanna J. Phillips ◽  
Anjan Misra ◽  
Burt G. Feuerstein ◽  
Sandeep Kunwar ◽  
Tarik Tihan

Abstract The pituicytoma is a rare neoplasm whose histogenesis is debated partly because of the diversity of tissue types present in the sellar region. In this article we illustrate the characteristic histologic, immunohistologic, and ultrastructural features of this unique neoplasm. Furthermore, we use array-based comparative genomic hybridization to demonstrate a unique pattern of genomic copy number aberrations in pituicytomas. Tumors were composed of bipolar, spindle cells that were immunopositive for S100, vimentin, and Bcl-2 and immunonegative for synaptophysin, chromogranin, and glial fibrillary acidic protein. Ultrastructural analysis was remarkable for absence of secretory granules. Array comparative genomic hybridization demonstrated genomic copy number imbalances, including losses on chromosome arms 1p, 14q, and 22q and gains on 5p. This pattern of genetic changes only partially overlaps with the genomic alterations reported in pituitary adenomas. In summary, our data suggest that pituicytomas are a unique subset of tumors of the sellar region.


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