PAX-8

PAX-8 along with PAX-2 are transcription factors (nuclear expression) important in the development of Mullein system, kidney, and thyroid.  They both are expressed in normal kidney and most renal neoplasms.  PAX-8 expression may also be seen in carcinomas of the lower urinary tract and nephrogenic adenomas.  In the study by Ozacan et. al., PAX-8 had better performance characteristics than PAX-2.
 
PAX-8 is not expressed in cancers from rectum, pituitary, adrenal, colon, prostate, breast, lung, stomach, liver, soft tissue, melanoma, and lymphoma.  The rabbit monoclonal PAX-8 antibody shows staining in lymph nodes, pancreas, and stomach/colon neuroendocrine cells.  The mouse PAX-8 antibody clone BC12 does not appear to have expression in lymph nodes, pancreas and stomach/colon neuroendocrine cells. (Tacha, D., et. al.)  In an experience by Ortiz-Rey, et al., they found PAX-8 to be helpful in differentiated seminal vesicle epithelium from prostate epithelium in needle core biopsies.  Sometimes this can be difficult to differentiate from carcinoma, and could be helpful in a panel to differentiate epithelial types.
 
Ozcan, A., et. al.
Tumor Type
No.
PAX-2
PAX-8
Renal Cell Carcinoma
 
 
 
     Clear Cell
95
95%
97%
     Papillary
38
76%
100%
     Chromophobe
25
56%
88%
     Collecting Duct
7
43%
71%
     Acquired Cystic Kidney
     Disease-related RCC
8
75%
100%
     Oncocytoma
13
54%
85%
 
Galley, M.P., et. al.
Tumor Type
PAX-8 (%)
Uterine Cervix SCC
3%
Urothelial Carcinoma
10%
 
Normal Tissue Expression for PAX-8  (Chan, J.K.C.)
Tissue
Expression Pattern
Thyroid
Follicular epithelium
Kidney
Tubular epithelium and Bowman capsule lining cells
Female Genital Tract
Ovary – inclusion cysts, rete ovarii, not surface mesothelium
Fallopian Tube – epithelium
Uterus – epithelium
Endocervix – epithelium (weak to moderate staining)
Male Genital Tract
Epithelium from tete testis to ejaculatory duct
Thymus
Thymic epithelium (weak staining)
Pancreas
Islet cells (rabbit polyclonal ab, mouse clone BC12 does not appear to cross react)
Lymphocytes
Subset of lymphoid cells, thought to be due to cross-reactivity with PAX-5 (rabbit polyclonal ab, mouse clone BC12 does not appear to cross react)
 
References:
Shen, SS. “Role of Immunohistochemistry in Diagnosing Renal Neoplams: When Is It Really Useful?”Arch Pathol Lab Med, Vol. 136, April 2012.  pp. 410-417. 
 
Al-Ghawi, H., Asojo, O. A., Truong, L. D., Ro, J. Y., Ayala, A. G., & Zhai, Q. J. (2010). Application of Immunohistochemistry to the Diagnosis of Kidney Tumors. Pathology Case Reviews, 15(1), 25–34. doi:10.1097/PCR.0b013e3181d51c70 
 
Ozcan, A., la Roza, de, G., Ro, J. Y., Shen, S. S., & Truong, L. D. (2012). PAX2 and PAX8 expression in primary and metastatic renal tumors: a comprehensive comparison. Archives of Pathology & Laboratory Medicine, 136(12), 1541–1551. doi:10.5858/arpa.2012-0072-OA 
 
Chan, J. K. C. (2013). Newly Available Antibodies With Practical Applications in Surgical Pathology. International Journal of Surgical Pathology, 21(6), 553–572. doi:10.1177/1066896913507601 
 
Gailey, M. P., & Bellizzi, A. M. (2013). Immunohistochemistry for the novel markers glypican 3, PAX8, and p40 (ΔNp63) in squamous cell and urothelial carcinoma. American Journal of Clinical Pathology, 140(6), 872–880. doi:10.1309/AJCP4NSKW5TLGTDS 
 
Tacha, D., Qi, W., Zhou, D., Bremer, R., & Cheng, L. (2013). PAX8 mouse monoclonal antibody [BC12] recognizes a restricted epitope and is highly sensitive in renal cell and ovarian cancers but does not cross-react with b cells and tumors of pancreatic origin. Applied Immunohistochemistry & Molecular Morphology : AIMM / Official Publication of the Society for Applied Immunohistochemistry, 21(1), 59–63. doi:10.1097/PAI.0b013e318257cc1c 
 
Ortiz-Rey – PAX8 AIMM editorial