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Tumor-associated trypsin inhibitor in patients with chronic pancreatic diseases.

作者信息

Plebani M, Basso D, Fabris C, Meggiato T, Del Favero G, Panozzo M P, Fogar P, Faggian D, Angonese C, Burlina A

机构信息

Istituto di Medicina Interna (Cattedra di Malattie Apparato Digerente), Università degli Studi di Padova, Italia.

出版信息

Klin Wochenschr. 1989 Oct 17;67(20):1029-32. doi: 10.1007/BF01727004.

DOI:10.1007/BF01727004
PMID:2586008
Abstract

Serum TATI (tumor-associated trypsin inhibitor) was measured in 41 control subjects, 30 patients with pancreatic cancer, 53 with chronic pancreatitis, and 47 with extrapancreatic diseases, mainly of gastrointestinal origin. TATI was found to be elevated in some subjects in all groups of patients; patients with chronic pancreatitis studied during an acute exacerbation of the disease had the highest percentage (68%) of pathological values. TATI was found to be correlated with elastase 1, tissue polypeptide antigen, and total and pancreatic isoamylase. A significant relationship was also found between TATI and serum creatinine levels.

摘要

相似文献

1
Tumor-associated trypsin inhibitor in patients with chronic pancreatic diseases.
Klin Wochenschr. 1989 Oct 17;67(20):1029-32. doi: 10.1007/BF01727004.
2
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Minerva Med. 1989 Mar;80(3):199-203.
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[Serum pancreatic secretory trypsin inhibitor (PSTI), amylase activity and pancreatic isoamylase activity in pancreatic diseases].
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Radioimmunoassay for human pancreatic secretory trypsin inhibitor: measurement of serum pancreatic secretory trypsin inhibitor in normal subjects and subjects with pancreatic diseases.人胰腺分泌型胰蛋白酶抑制剂的放射免疫测定:正常受试者和胰腺疾病患者血清胰腺分泌型胰蛋白酶抑制剂的测定
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Correlation between serum concentrations of three specific exocrine pancreatic proteins and pancreatic duct morphology at ERCP examinations.ERCP检查时三种特定胰腺外分泌蛋白血清浓度与胰管形态之间的相关性
Scand J Gastroenterol. 1984 Mar;19(2):220-7.

引用本文的文献

1
Tumour-associated trypsin inhibitor in the diagnosis of pancreatic carcinoma.肿瘤相关胰蛋白酶抑制剂在胰腺癌诊断中的应用
J Cancer Res Clin Oncol. 1994;120(8):494-7. doi: 10.1007/BF01191804.

本文引用的文献

1
Some statistical methods useful in circulation research.一些在循环研究中有用的统计方法。
Circ Res. 1980 Jul;47(1):1-9. doi: 10.1161/01.res.47.1.1.
2
Purification and characterization of a tumor-associated trypsin inhibitor from the urine of a patient with ovarian cancer.从一名卵巢癌患者尿液中纯化并鉴定一种肿瘤相关胰蛋白酶抑制剂。
J Biol Chem. 1982 Nov 25;257(22):13713-6.
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Protein inhibitors of proteinases.蛋白酶的蛋白质抑制剂。
Annu Rev Biochem. 1980;49:593-626. doi: 10.1146/annurev.bi.49.070180.003113.
4
Elimination of pancreatic secretory trypsin inhibitor from the circulation. A study in man.循环中胰腺分泌性胰蛋白酶抑制剂的清除。一项人体研究。
Scand J Gastroenterol. 1983 Oct;18(7):955-9. doi: 10.3109/00365528309182122.
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Serum pancreatic secretory trypsin inhibitor in pancreatic disease.胰腺疾病中的血清胰分泌性胰蛋白酶抑制剂
Clin Chim Acta. 1984 Sep 29;142(2):231-40. doi: 10.1016/0009-8981(84)90381-4.
6
Excretion of a tumor-associated trypsin inhibitor (TATI) in urine of patients with gynecological malignancy.妇科恶性肿瘤患者尿液中肿瘤相关胰蛋白酶抑制剂(TATI)的排泄情况。
Int J Cancer. 1983 Jun 15;31(6):711-4. doi: 10.1002/ijc.2910310606.
7
Radioimmunoassay for human pancreatic secretory trypsin inhibitor: measurement of serum pancreatic secretory trypsin inhibitor in normal subjects and subjects with pancreatic diseases.人胰腺分泌型胰蛋白酶抑制剂的放射免疫测定:正常受试者和胰腺疾病患者血清胰腺分泌型胰蛋白酶抑制剂的测定
Clin Chim Acta. 1980 Apr 25;103(2):135-43. doi: 10.1016/0009-8981(80)90205-3.
8
Optimized conditions for determining activity concentration of alpha-amylase in serum, with 1,4-alpha-D-4-nitrophenylmaltoheptaoside as substrate.以1,4-α-D-4-硝基苯基麦芽庚糖苷为底物测定血清中α-淀粉酶活性浓度的优化条件。
Clin Chem. 1985 Jan;31(1):14-9.
9
Tumour-associated trypsin inhibitor, TATI, in patients with pancreatic cancer, pancreatitis and benign biliary diseases.肿瘤相关胰蛋白酶抑制剂(TATI)在胰腺癌、胰腺炎及良性胆道疾病患者中的情况
Br J Cancer. 1986 Aug;54(2):297-303. doi: 10.1038/bjc.1986.176.
10
Pancreatic secretory trypsin inhibitor from human amniotic fluid and fetal and neonatal urine: concentrations and physicochemical characterization.来自人羊水、胎儿及新生儿尿液的胰腺分泌型胰蛋白酶抑制剂:浓度及理化特性
Clin Chim Acta. 1986 Apr 30;156(2):123-9. doi: 10.1016/0009-8981(86)90145-2.