TY - JOUR
T1 - TGF-alpha immunoreactivity in laryngeal carcinoma
T2 - Lack of prognostic value and correlation to EGF-receptor expression
AU - Lee, C. Soon
AU - Redshaw, Anna
AU - Boag, Guy
PY - 1996
Y1 - 1996
N2 - Background: Transforming growth factor alpha (TGF-α) is a polypeptide that is structurally similar to epidermal growth factor (EGF) that binds to the epidermal growth factor receptor (EGFR) and has been implicated in the development of several types of human tumours. Methods: The expression of TGF-α is examined in laryngeal squamous cell carcinomas (SCC) (n = 24) and non-neoplastic polyps (n = 7) using streptavidin-biotin immunohistochemistry and a monoclonal antibody to the TGF-α protein. These cases had been previously characterized for EGFR immunoreactivity. The carcinomas were classified as well differentiated (n = 2), moderately differentiated (n = 16) and poorly differentiated (n = 6). Tissues from metastatic tumour deposits in lymph nodes (n = 5) were also studied. Results: TGF-α overexpression was defined as intense immunoreactivity in more than two-thirds of tumour cells immunostained for TGF-α and was present in the majority of the SCC cases (n = 15; 63%) and metastatic tumour deposits (n = 4; 80%). In contrast, although some of the cord polyps showed weak (n = 2) to moderate (n = 5) immunostaining, none had evidence of strong TGF-α immunoreactivity. The differences in TGF-α immunoreactivity were significant between primary laryngeal SCC and vocal cord polyps (P = 0.013; χ test with continuity correction), and between metastatic laryngeal SCC and vocal cord polyps (P = 0.023; χ2 test with continuity correction). There was no significant difference in TGF-α expression between the different grades of carcinomas (P = 0.92, χ2 test) or between non-metastatic and metastatic carcinomas (P = 0.82; χ2 test with continuity correction). No significant correlation was found between TGF-α expression and patient survival or tumour recurrence (r = 0.077, r2 = 0.006, P = 0.75; simple regression analysis), or between TGF- α expression and EGFR immunoreactivity (r = 0.325, r2 = 0.106, P = 0.0851). Conclusions: In conclusion, increased TGF-α immunoreactivity is present in most cases of laryngeal SCC with specific relationship to tumour grade, suggesting that in may be important in the development of laryngeal carcinomas but not in its progression. NO significant correlation was found between TGF-α and EGFR expression in laryngeal tumours and TGF-α immunoreactivity is of no prognostic value.
AB - Background: Transforming growth factor alpha (TGF-α) is a polypeptide that is structurally similar to epidermal growth factor (EGF) that binds to the epidermal growth factor receptor (EGFR) and has been implicated in the development of several types of human tumours. Methods: The expression of TGF-α is examined in laryngeal squamous cell carcinomas (SCC) (n = 24) and non-neoplastic polyps (n = 7) using streptavidin-biotin immunohistochemistry and a monoclonal antibody to the TGF-α protein. These cases had been previously characterized for EGFR immunoreactivity. The carcinomas were classified as well differentiated (n = 2), moderately differentiated (n = 16) and poorly differentiated (n = 6). Tissues from metastatic tumour deposits in lymph nodes (n = 5) were also studied. Results: TGF-α overexpression was defined as intense immunoreactivity in more than two-thirds of tumour cells immunostained for TGF-α and was present in the majority of the SCC cases (n = 15; 63%) and metastatic tumour deposits (n = 4; 80%). In contrast, although some of the cord polyps showed weak (n = 2) to moderate (n = 5) immunostaining, none had evidence of strong TGF-α immunoreactivity. The differences in TGF-α immunoreactivity were significant between primary laryngeal SCC and vocal cord polyps (P = 0.013; χ test with continuity correction), and between metastatic laryngeal SCC and vocal cord polyps (P = 0.023; χ2 test with continuity correction). There was no significant difference in TGF-α expression between the different grades of carcinomas (P = 0.92, χ2 test) or between non-metastatic and metastatic carcinomas (P = 0.82; χ2 test with continuity correction). No significant correlation was found between TGF-α expression and patient survival or tumour recurrence (r = 0.077, r2 = 0.006, P = 0.75; simple regression analysis), or between TGF- α expression and EGFR immunoreactivity (r = 0.325, r2 = 0.106, P = 0.0851). Conclusions: In conclusion, increased TGF-α immunoreactivity is present in most cases of laryngeal SCC with specific relationship to tumour grade, suggesting that in may be important in the development of laryngeal carcinomas but not in its progression. NO significant correlation was found between TGF-α and EGFR expression in laryngeal tumours and TGF-α immunoreactivity is of no prognostic value.
KW - EGF-receptor
KW - immunohistochemistry
KW - laryngeal neoplasms
KW - TGF-α
KW - tumour markers
KW - tyrosine kinase
UR - http://www.scopus.com/inward/record.url?scp=0029999803&partnerID=8YFLogxK
U2 - 10.1111/j.1445-2197.1996.tb00783.x
DO - 10.1111/j.1445-2197.1996.tb00783.x
M3 - Article
C2 - 8678876
AN - SCOPUS:0029999803
SN - 0004-8682
VL - 66
SP - 464
EP - 468
JO - Australian and New Zealand Journal of Surgery
JF - Australian and New Zealand Journal of Surgery
IS - 7
ER -