The presence of the proteolysis-inducing factor in urine does not predict the malignancy of a pancreatic tumour
© Teichs et al; licensee BioMed Central Ltd. 2005
Received: 10 February 2005
Accepted: 21 June 2005
Published: 21 June 2005
The proteolysis-inducing factor (PIF) was identified as a tumour product in various gastrointestinal cancers. A previous study in pancreatic cancer patients suggested PIF expression as a tumour marker, which is not related to tumour size. We hypothesized that PIF could be a useful marker to exclude benign pancreatic tumors, as chronic pancreatitis with a pancreatic mass.
Urine of patients with a pancreatic mass of uncertain malignancy was investigated for PIF expression by Western blot. Sufficient urine protein for analysis was available in 59 patients. The diagnosis was established by histology in 54 patients and by follow up in five patients with chronic pancreatitis. In addition, serum CA19-9 was measured.
The sensitivity (specifity) for the detection of a malignant pancreatic tumour was 90% (75%) and 54% (71%) for CA19-9 and PIF, respectively. The sensitivity (specifity) for the distinction of pancreatic cancer from chronic pancreatitis was 89% (80%) and 57% (63%) for CA19-9 and PIF, respectively.
Evaluation of PIF in urine is of no diagnostic value in patients with a pancreatic mass of unknown malignancy.
Distinction between benign and malignant pancreatic tumours is still difficult, despite significant progress in imaging techniques. Patients with chronic pancreatitis are at increased risk to develop pancreatic cancer . Pancreatic inflammation, as observed in chronic pancreatitis, can be mistaken on imaging as cancer and inversely. Serum carbohydrate antigen 19-9 (CA19-9) levels are elevated in 80% of pancreatic cancer patients, but can also be increased in 20% of patients with chronic pancreatitis . An accurate and non-invasive test to differentiate pancreatic cancer from chronic pancreatitis is not available.
Cancer frequently induces cachexia, but not all cancer patients will develop cachexia. This is not necessarily a late phenomenon in tumour progression. It may be present at diagnosis and may be the leading symptom that induces search for a tumour. A study of pancreatic cancer patients revealed that patients had lost a median of about 14% of their usual body weight at the time of diagnosis, and that this weight loss was progressive, increasing to a median of 25% at the time of the last assessment . The central role in this process of – predominant – skeletal muscle waste seems to play the proteolysis-inducing factor (PIF) .
PIF is a 24-kDa sulphated glycoprotein synthesized by cachexia-inducing murine and human tumours, which induces catabolism of myofibrillar proteins in skeletal muscle via a direct stimulation of the proteasome pathway in muscle cells . Administration of PIF to normal mice leads to a rapid decrease in body weight, which is based primarily on a loss of skeletal muscle mass [4, 6].
PIF is expressed in a variety of gastrointestinal cancers . It was detected in the urine of 44 from 55 pancreatic cancer patients, who had a significantly greater total weight loss and rate of weight loss than patients whose urine did not contain PIF. Interestingly, PIF expression was not dependent on cancer stage, but seemed to be a qualitative marker of pancreatic cancer: even stage 2 tumours expressed PIF in 83 per cent .
PIF has not been investigated in benign pancreatic diseases. We therefore hypothesized that PIF production in patients with a pancreatic tumour would clearly indicate the malignant nature of the disease. Special attention was paid to a clear distinction to a pancreatic mass caused by chronic pancreatitis.
100 patients with a pancreatic mass of uncertain malignancy (detected by computed tomography, magnet resonance tomography, ultrasound and/or endoscopic retrograde cholangiopancreaticography) were investigated. Patients with UICC stage 4 (locally extended and metastasised disease) were not enrolled. After collection of urine from all study participants, we investigated 30 ml urine for the presence of PIF with a specific mouse monoclonal antibody in a Western blot setting as described recently [4, 8]. In brief, urine protein was precipitated with ammonium sulphate and dialysed against water between 12 and 15 hours (overnight) with a molecular weight cut-off of 10 kD (Slide-A-Lyzer Dialysis Cassette). 5 μg of concentrated samples were separated with sodium dodecylsulphate polyacrylamide gel electrophoresis and subsequently blotted on nitrocellulose membranes. After incubation with 10 μg/ml of the mouse monoclonal PIF antibody (provided with courtesy by MJ Tisdale) and streptavidine horseradish peroxidase conjugate, the bands were detected using the Fluorescent ECL Plus system (Amersham). In addition, CA19-9 in serum was measured with an electrochemiluminescence immunoassay (CA19-9®Roche Diagnostics or ADVIA Centaur®, Bayer Healthcare), the upper limit of normal was 22 U/ml. The ethics committees of the three participating centres approved this protocol.
Results and discussion
Diagnostic values of PIF in comparison to CA19-9 to discriminate malignant vs. benign and pancreatic cancer (PaCa) vs. chronic pancreatitis (CP).
all malignant vs. all benign
PaCa vs. CP
positive predictive value
negative predictive value
This is the first attempt to evaluate the proteolysis-inducing factor as a diagnostic marker of pancreatic cancer in patients with a potentially resectable pancreatic tumour. We found a weak association with malignancy, but the diagnostic value to distinguish benign from malignant pancreatic tumours is lower than CA19-9. PIF seems to be of a rather limited importance to answer this question in every-day care.
A major drawback of our data is the high amount of patients with insufficient urinary protein after extraction and dialysis. For practical reasons in this multi-centre collaboration, we tried to investigate PIF in a small urine sample, as initially suggested by Todorov et al. . Our problem could be potentially solved by the collection of higher urine volumes in further studies.
PIF was detected in 6 patients with chronic pancreatitis without evidence for a malignancy by 12 months follow up or histology. This raises the question about the origin of PIF in these patients. Although the majority of investigations found PIF expression only in tumour tissue, the expression of PIF in non-malignant tissue has been also reported . The primary role of PIF seems to be in regulation of development . After cloning of the cDNA for PIF, a human homologue – the human cachexia associated protein (HCAP) – has been identified, which is minimally expressed in normal tissues [10, 11]. It can be speculated, that the ongoing inflammation in patients with chronic pancreatitis is capable to generate PIF. This could explain the low specifity of PIF to detect pancreatic malignancies in our study. Three patients with pancreatic cancer had normal CA19-9 values, two of them were PIF-positive. A sequential testing of PIF in the case of a CA19-9-negative pancreatic tumour may be beneficial but has to be considered cautiously based on these small patient numbers. However, even this approach would fail to detect all pancreatic cancer patients in our study.
Although our data indicate that PIF is not helpful as a diagnostic marker of pancreatic cancer, a benefit may be the early identification of patients who need nutritional intervention . In previous studies the detection of PIF was associated with prior weight loss. PIF induces an increase of the ubiquitin – proteasome activity resulting in protein catabolism. Administration of the polyunsaturated fatty acid eicosapentaenoic acid (EPA) attenuates protein degradation by antagonizing the PIF induced up regulation of the ubiquitin – proteasome proteolytic pathway in cachectic tumour bearing mice . A first randomised placebo – controlled trial in patients with pancreatic cancer suggest that a EPA enriched oral supplement has the potential to induce a net gain of weight, lean body mass and improvement of quality of life .
PIF is not superior to the established tumour marker CA19-9 to distinguish benign from malignant pancreatic tumours. Further investigations should clarify whether the onset of PIF expression in the long-term follow-up of chronic pancreatitis patients is associated with early malignancy and whether it precedes morphologic and clinical signs of pancreatic cancer. In future, the evaluation of PIF as an indicator for early nutritional intervention seems to be warranted.
carbohydrate antigen 19-9
We thank Professor M.J. Tisdale for kindly providing the anti-PIF-antibody. We furthermore thank S. Kistner and T. Herrmann for expert technical assistance.
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