TY - JOUR
T1 - Basaloid squamous cell carcinoma of the esophagus
T2 - Assessment for high-risk human papillomavirus and related molecular markers
AU - Bellizzi, Andrew M.
AU - Woodford, Randall L.
AU - Moskaluk, Christopher A.
AU - Jones, David R.
AU - Kozower, Benjamin D.
AU - Stelow, Edward B.
PY - 2009/11
Y1 - 2009/11
N2 - Basaloid squamous cell carcinoma (BSCC) of the esophagus is rare, historically confused for adenoid cystic carcinoma, and recently shown to behave similar to conventional, keratinizing esophageal squamous cell carcinoma. At other sites (eg, oropharynx, anogenital tract) the basaloid phenotype is frequently associated with the presence of high-risk human papillomavirus (HPV). HPVs role in esophageal squamous cell carcinomas is less certain, and to our knowledge, a direct examination of esophageal BSCC for high-risk HPV has not been performed earlier. Nine cases of esophageal BSCC were retrieved from our surgical pathology files. Twenty-two cases of keratinizing esophageal squamous cell carcinoma served as controls. In situ hybridization (ISH) for high-risk HPV and immunohistochemistry for related molecular markers including p53, cyclin D1, and p16 (scored 0 to 4+ based on percentage of cells staining; p53 additionally scored for intensity) were performed. HPV ISH was nonreactive in all tested cases. Compared with controls, BSCC showed less immunoreactivity for p16 and p53 (P=0.003, 0.009). Esophageal BSCC is negative for high-risk HPV by ISH, distinguishing these lesions from other BSCCs. Differential p16 and p53 expression in BSCC suggests that these tumors are molecularly distinct from conventional esophageal squamous cell carcinomas.
AB - Basaloid squamous cell carcinoma (BSCC) of the esophagus is rare, historically confused for adenoid cystic carcinoma, and recently shown to behave similar to conventional, keratinizing esophageal squamous cell carcinoma. At other sites (eg, oropharynx, anogenital tract) the basaloid phenotype is frequently associated with the presence of high-risk human papillomavirus (HPV). HPVs role in esophageal squamous cell carcinomas is less certain, and to our knowledge, a direct examination of esophageal BSCC for high-risk HPV has not been performed earlier. Nine cases of esophageal BSCC were retrieved from our surgical pathology files. Twenty-two cases of keratinizing esophageal squamous cell carcinoma served as controls. In situ hybridization (ISH) for high-risk HPV and immunohistochemistry for related molecular markers including p53, cyclin D1, and p16 (scored 0 to 4+ based on percentage of cells staining; p53 additionally scored for intensity) were performed. HPV ISH was nonreactive in all tested cases. Compared with controls, BSCC showed less immunoreactivity for p16 and p53 (P=0.003, 0.009). Esophageal BSCC is negative for high-risk HPV by ISH, distinguishing these lesions from other BSCCs. Differential p16 and p53 expression in BSCC suggests that these tumors are molecularly distinct from conventional esophageal squamous cell carcinomas.
KW - Basaloid squamous cell carcinoma
KW - Cyclin D1
KW - Esophagus
KW - High-risk
KW - Human papillomavirus
KW - Immunohistochemistry
KW - In situ hybridization
KW - Oncoprotein
KW - P16
KW - P53
KW - Tumor suppressor
UR - http://www.scopus.com/inward/record.url?scp=70350448230&partnerID=8YFLogxK
U2 - 10.1097/PAS.0b013e3181b46fd4
DO - 10.1097/PAS.0b013e3181b46fd4
M3 - Article
C2 - 19738459
AN - SCOPUS:70350448230
SN - 0147-5185
VL - 33
SP - 1608
EP - 1614
JO - American Journal of Surgical Pathology
JF - American Journal of Surgical Pathology
IS - 11
ER -