Original ArticlesLewis Y antigen expression and postoperative survival in non–small cell lung cancer
Section snippets
Material and methods
A total of 237 consecutive patients with pathologic stage 1–3a NSCLC who underwent complete tumor resection and mediastinal lymph node dissection without chemotherapy nor radiation therapy before operation at the Department of Thoracic Surgery, Chest Disease Research Institute, Kyoto University between January 1, 1985 and December 31, 1990, were reviewed. Complete tumor resection was defined when no microscopic cancers were identified either in the resection margins of the tumor or in the
Expression of LeY
The number of patients for whom the grade of LeY expression was judged (−), (+), (2+), (3+), (4+), or (5+) was 57 (24.2%), 17 (7.2%), 42 (17.8%), 51 (21.6%), 31 (13.1%), and 38 (16.1%), respectively. The 5-year survival rates were 50.2% for (−) group, 79.3% for (1+) group, 80.0% for (2+) group, 74.4% for (3+) group, 76.0% for (4+) group, and 77.6% for (5+) group. The LeY expression (−) group showed significantly worse postoperative prognosis than the other (+), (2+), (3+), (4+), and (5+)
Discussion
During neoplastic transformation, glycosylation may revert to an earlier development form with lung cancer cells reexpressing antigens found on immature embryonic lung cells. The tumor-associated LeY is the focus of the present study and is correlated with postoperative survival.
Several findings have been reported with respect to LeY expression in normal tissue and in cancer tissue since the 1980s, when various kinds of MoAbs against LeY were generated. As for LeY expression in lung cancer,
Acknowledgements
We thank Dr Nobuyuki Hamajima, Division of Epidemiology, Aichi Cancer Institute, Aichi, Japan, for his helpful comment and critical reading of the statistical section of the manuscript.
References (19)
- et al.
Novel fucolipids of human adenocarcinomacharacterization of the major Ley antigen of human adenocarcinoma as trifucosylnonaosyl Ley glycolipid (III3FucV3FucVI2FucnLc6)
J Biol Chem
(1986) - et al.
Expression of Lewis-related antigen and prognosis in stage I non-small cell lung cancer
Ann Thorac Surg
(1995) - et al.
Time trends and survival after surgery for primary lung cancer during 1976–1990
J Thorac Cardiovasc Surg
(1996) - et al.
Expression of Lewisa, Lewisb, X, and Y blood group antigens in human colonic tumors and normal tissue and in human tumor-derived cell lines
Cancer Res
(1986) - et al.
Association of sialyl-Lewisa and sialyl-Lewisx with MUC-1 apomucin in a pancreatic cancer cell lines
Cancer Res
(1995) - et al.
Lewisx- and sialyl Lewisx-related antigen expression in human malignant and nonmalignant colonic tissues
Cancer Res
(1986) - et al.
Increased expression of sialyl-dimeric Lex antigen in liver metastasis of human colorectal carcinoma
Cancer Res
(1989) - et al.
Increased expression of sialyl Lewisx antigen correlates with poor survival in patients with colorectal carcinomaclinicopathological immunohistochemical study
Cancer Res
(1993) - et al.
Differential expression of difucosyl type 2 chain (Ley) defined by monoclonal antibody AH6 in different locations of colonic epithelia, various histological types of colonic polyps and adenocarcinomas
Cancer Res
(1986)
Cited by (29)
Fucosyltransferase 4 shapes oncogenic glycoproteome to drive metastasis of lung adenocarcinoma
2020, EBioMedicineCitation Excerpt :On the other hand, the clinical significance of fucosyltransferases involved in terminal fucosylation (α1,3- or α1,4- linkage) in lung cancer remains controversial. Past studies have demonstrated aberrant expression of terminal fucosylated epitopes such as Lewis antigens in non-small cell lung cancer tissues [8–10]. Nevertheless, the prognostic values of various Lewis antigens appeared to differ.
Primary lung carcinoma arising from emphysematous bullae
2002, Lung CancerThe role of blood group antigens in malignant progression, apoptosis resistance, and metastatic behavior
2000, Transfusion Medicine Reviews