Involvement of interleukin-6 in the elevation of plasma fibrinogen levels in lung cancer patients

被引:66
作者
Yamaguchi, T [1 ]
Yamamoto, Y [1 ]
Yokota, S [1 ]
Nakagawa, M [1 ]
Ito, M [1 ]
Ogura, T [1 ]
机构
[1] Toneyama Natl Hosp, Dept Internal Med, Toyonaka, Osaka 5608552, Japan
关键词
IL-6; CRP; fibrinogen; FDP; lung cancer patients;
D O I
10.1093/jjco/28.12.740
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: involvements of interleukin-6 (IL-6) and fibrinogen in cancer development have been independently studied. However, the association of these molecules in cancer patients remains uncertain. This study was conducted to clarify the association according to the clinicopathological characteristics of lung cancer patients. Methods: Serum IL-6 levels assayed in 339 patients without pleural effusion were assessed according to clinical stage, histological type of the cancer and levels of fibrin (ogen) degradation products (FDP), and C-reactive protein (CRP), Results: Elevations of serum IL-6 levels more than 4 pg/ml were found in 37.8% of all patients. According to the clinical stage and histological type, the elevations were significantly more frequent in the advanced stage (44.7%), in squamous cell (49.1%) and large cell carcinomas (63.6%). Similarly, the frequency of the elevated cases (>400 mg/dl) and the mean value of, the fibrinogen level were also higher in the advanced stage (54.2%, 455.0 mg/dl) and large cell carcinoma (54.6%, 469.3 mg/dl), respectively. The elevations of fibrinogen, FDP and CRP levels were found to be related to those of the IL-6 level. Conclusion: In lung cancer, serum IL-6 elevations are particularly Frequent in the advanced stages of patients with squamous cell and large cell carcinoma, which are associated with the elevated levels of fibrinogen, suggesting a possibility that IL-6 was involved not only directly, but also indirectly, through regulating plasma fibrinogen with promotion of cancer development in vivo.
引用
收藏
页码:740 / 744
页数:5
相关论文
共 32 条
[1]   INHIBITION BY FIBRIN COAGULATION OF LUNG-CANCER CELL DESTRUCTION BY HUMAN INTERLEUKIN-2-ACTIVATED KILLER-CELLS [J].
ATAGI, S ;
SONE, S ;
FUKUTA, K ;
OGURA, T .
JAPANESE JOURNAL OF CANCER RESEARCH, 1992, 83 (10) :1088-1094
[2]  
BAFFET G, 1991, MOL BIOL MED, V8, P141
[3]  
Basolo F, 1996, CANCER RES, V56, P3118
[4]  
BLAY JY, 1993, BLOOD, V82, P2261
[5]  
BLAY JY, 1992, CANCER RES, V52, P3317
[6]  
COSTANTINI V, 1991, CANCER RES, V51, P349
[7]   ABNORMALITIES OF BLOOD-COAGULATION TESTS IN PATIENTS WITH CANCER [J].
EDWARDS, RL ;
RICKLES, FR ;
MORITZ, TE ;
HENDERSON, WG ;
ZACHARSKI, LR ;
FORMAN, WB ;
CORNELL, CJ ;
FORCIER, RJ ;
ODONNELL, JF ;
HEADLEY, E ;
KIM, SH ;
ODELL, R ;
TORNYOS, K ;
KWAAN, HC .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1987, 88 (05) :596-602
[8]  
Katsumata N, 1996, CLIN CANCER RES, V2, P553
[9]   THE BIOLOGY OF INTERLEUKIN-6 [J].
KISHIMOTO, T .
BLOOD, 1989, 74 (01) :1-10
[10]   Increased release of interleukin-1 beta, interleukin-6, and tumor necrosis factor-alpha by bronchoalveolar cells lavaged from involved sites in pulmonary tuberculosis [J].
Law, K ;
Weiden, M ;
Harkin, T ;
TchouWong, KM ;
Chi, CX ;
Rom, WN .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (02) :799-804