TY - JOUR
T1 - 15-Lipoxygenase-2 expression in benign and neoplastic lung
T2 - An immunohistochemical study and correlation with tumor grade and proliferation
AU - Gonzalez, Adriana L.
AU - Roberts, Richard L.
AU - Massion, Pierre P.
AU - Olson, Sandra J.
AU - Shyr, Yu
AU - Shappell, Scott B.
N1 - Funding Information:
Supported in part by National Institutes of Health Specialized Program of Research Excellence (SPORE) for Lung Cancer, 1 P50 CA090949 (A.L.G., P.P.M.), and by a Discovery Grant from the Vanderbilt Ingram Cancer Center (S.B.S.). P.M. is supported by a Merit Review Entry Program Award from the Veterans Administration.
PY - 2004/7
Y1 - 2004/7
N2 - 15-Lipoxygenase-2 (15-LOX-2) is an arachidonic acid-metabolizing enzyme expressed in prostate, lung, skin, esophagus, and cornea. In the benign prostate, it is expressed in differentiated secretory epithelial cells, where its enzymatic product 15-HETE may regulate transcription by activating the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARγ). 15-LOX-2 and 15-HETE formation are reduced in prostate carcinoma. The distribution of 15-LOX-2 in the normal lung and its expression in lung carcinomas has not been reported and was investigated in the current study by using immunohistochemistry and tissue microarrays (TMAs). In benign lung, 15-LOX-2 immunostaining was noted exclusively in type II pneumocytes, which are known to express PPARγ. Of 160 lung carcinomas, 15-LOX-2 was expressed in non-small cell carcinomas (NSCLC), including 33 of 69 (48%) adenocarcinomas, with 10 of 16 (63%) bronchioloalveolar carcinomas immunopositive. Fourteen of 55 (25%) squamous cell carcinomas and 2 of 14 (14%) large cell carcinomas showed weak immunostaining. All 19 neuroendocrine tumors were negative. Better differentiated NSCLCs showed greater 15-LOX-2 expression, with a significant inverse correlation between 15-LOX-2 immunostaining and tumor grade (P < 0.03). A significant inverse correlation was also noted between 15-LOX-2 immunostaining and tumor cell proliferation (Ki-67 immunostaining; P < 0.0001). These findings suggest a possible role of 15-LOX-2 in regulating secretory differentiation and proliferation in benign lung and NSCLCs, particularly adenocarcinomas.
AB - 15-Lipoxygenase-2 (15-LOX-2) is an arachidonic acid-metabolizing enzyme expressed in prostate, lung, skin, esophagus, and cornea. In the benign prostate, it is expressed in differentiated secretory epithelial cells, where its enzymatic product 15-HETE may regulate transcription by activating the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARγ). 15-LOX-2 and 15-HETE formation are reduced in prostate carcinoma. The distribution of 15-LOX-2 in the normal lung and its expression in lung carcinomas has not been reported and was investigated in the current study by using immunohistochemistry and tissue microarrays (TMAs). In benign lung, 15-LOX-2 immunostaining was noted exclusively in type II pneumocytes, which are known to express PPARγ. Of 160 lung carcinomas, 15-LOX-2 was expressed in non-small cell carcinomas (NSCLC), including 33 of 69 (48%) adenocarcinomas, with 10 of 16 (63%) bronchioloalveolar carcinomas immunopositive. Fourteen of 55 (25%) squamous cell carcinomas and 2 of 14 (14%) large cell carcinomas showed weak immunostaining. All 19 neuroendocrine tumors were negative. Better differentiated NSCLCs showed greater 15-LOX-2 expression, with a significant inverse correlation between 15-LOX-2 immunostaining and tumor grade (P < 0.03). A significant inverse correlation was also noted between 15-LOX-2 immunostaining and tumor cell proliferation (Ki-67 immunostaining; P < 0.0001). These findings suggest a possible role of 15-LOX-2 in regulating secretory differentiation and proliferation in benign lung and NSCLCs, particularly adenocarcinomas.
UR - http://www.scopus.com/inward/record.url?scp=3142530344&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=3142530344&partnerID=8YFLogxK
U2 - 10.1016/j.humpath.2004.04.001
DO - 10.1016/j.humpath.2004.04.001
M3 - Article
C2 - 15257547
AN - SCOPUS:3142530344
SN - 0046-8177
VL - 35
SP - 840
EP - 849
JO - Human Pathology
JF - Human Pathology
IS - 7
ER -