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The alpha-fetoprotein (afp) receptor (recaf) is an oncofetal antigen found in most types of cancer. Using a competitive radioimmunoassay, we measured the concentration of serum recaf in three sets of samples.
Set 1 was blind and consisted of 119 normal subjects, 43 breast cancer patients (stages i and ii), and 20 patients with benign breast conditions. In this set, the assay discriminated normal from cancer samples with a receiver operating characteristic for the area under the curve (ROCAUC) of 0.983; with 95% specificity and 93% sensitivity at a cut-off of 4.6 K (arbitrary) recaf units; and with 72% sensitivity and 100% specificity at a cut-off of 7.3 K units. At 7.3 K units, the specificity for benign breast conditions was 85%, and the sensitivity was 72% (ROCAUC was 0.773). Carcinoembryonic antigen and cancer antigen 15-3 respectively showed 39% and 41% sensitivity, with 95% specificity in comparisons of normal with cancer samples, and 34% and 44% sensitivity, with 85% specificity in comparisons of benign with cancer samples. Set 2 consisted of 353 normal, 30 benign, and 64 cancer samples (stages ii and iii). The recaf assay sensitivity in discriminating normal from cancer samples was 97%, with 97% specificity. Benign compared with cancer samples showed 87% sensitivity, with 97% specificity. Set 3 included only 40 normal and 40 cancer samples. The assay sensitivity was 89%, with 100% specificity. Sets 2 and 3 were not tested with carcinoembryonic antigen and cancer antigen 15-3.
These results strongly suggest that the recaf assay could be used for detecting breast cancer in its early stages.
Alpha-fetoprotein (afp) is a major fetal serum protein 1–4 that is synthesized mainly by the yolk sac and liver 2,5. After birth, circulating levels of afp drop sharply, virtually disappearing from the blood of normal adult individuals 2.
Immature cells from most fetal structures internalize afp, and it has been suggested that the purpose of that internalization—and one of the functions of this protein—is to transport and deliver polyunsaturated fatty acids into fetal cells 6,7. The afp uptake ceases when embryonic cells and tissue structures approach a high degree of differentiation, even if the blood concentration of afp is still high or increasing 8–10.
In vitro and in vivo studies showed that malignant cells regain the ability to take up afp via a receptor that would be present in undifferentiated cells of either embryonic or tumour origin 10–15, but mostly absent in normal adult cells. The existence of such a receptor for afp (recaf) was then demonstrated and functionally characterized in several cell lines 16–18.
Because recaf is found in a variety of cancers and in fetal cells (but not in their mature counterparts), the receptor falls within the definition of a wide-spectrum oncofetal antigen with potential for cancer diagnosis, screening, and follow-up.
Previous immunohistology work using the same polyclonal antibodies described herein showed a clear difference in recaf staining between stomach cancer cells and nonmalignant cells 19, and recaf concentrations have been reported to be higher in serum from a variety of cancer patients than in serum from patients with benign proliferating diseases or from normal subjects 20.
In the present study, we describe a serum recaf radioimmunoassay that can detect the early stages of breast cancer. The test is capable of distinguishing cancer patients from healthy individuals—and from those with benign lesions—with a degree of accuracy so far unattainable with other cancer markers.
The MCF-7 human breast cancer cell line was obtained from the American Type Culture Collection (Manassas, VA, U.S.A.) and grown in rpmi medium containing 10% fetal calf serum. Before extraction, the cells were incubated for 1 hour at 37°C in serumfree rpmi medium to deplete them of bovine afp. The cells were then trypsinized and re-suspended at a concentration of 5×107 per millilitre of tbs medium (0.05 mol/L Tris–HCl plus 0.1 mol/L NaCl, pH 7.5). Next, the suspension was sonicated for 2 minutes in an ice bath using a Sonic Dismembrator (Thermo Fisher Scientific, Waltham, MA, U.S.A.) at 32 W, followed by centrifugation for 10 minutes at 14,000 rpm in an Eppendorf Microfuge (Eppendorf Canada, Mississauga, ON). The total protein concentration of the supernatants was 7–12 mg/mL as determined using a commercial protein assay (Total Protein: Bio-Rad Laboratory, Hercules, CA, U.S.A.). After 0.02% thimerosal was added, the cell extracts were stored at −20°C until used in the experiments.
Affinity chromatography on an afp-agarose column was used to purify the recaf. The afp was purified from the supernatant of HEP-2 culture medium by affinity chromatography using an anti-afp monoclonal antibody. One milliliter MCF-7 extract was incubated for 4 hours, at room temperature and under gentle agitation, with 10 mL afp-agarose in 0.05 mol/L Tris–HCl (pH 6.5). After thorough washing, the bound recaf was eluted using 0.8 mol/L KCl in the same buffer. The eluates were concentrated to 300–1000 μg/mL using a Centricom spin filter (Millipore Corporation, Billerica, MA, U.S.A.).
Rabbits were immunized intradermally with a 50:50 emulsion of 1 mg purified recaf in 1 mL of phosphate-buffered saline (pbs) and 1 mL Freund’s complete adjuvant. Two boosts, each containing 0.5 mg recaf in incomplete Freund’s adjuvant, were administered at 2-week intervals. The rabbits were bled from the ear vein 1 week after the last boost. The blood was allowed to clot overnight at room temperature, and the serum was centrifuged and stored at −30°C until further use. The immunoglobulin G fraction of the anti-recaf rabbit antiserum was isolated on a protein A Sepharose column (Sigma–Aldrich, St. Louis, Missouri, U.S.A.) according to the manufacturer’s instructions.
Polyacrylamide gels containing 10% sodium dodecylsulfate were used in a Bio-Rad polyacrylamide gel electrophoresis apparatus following the Laemmli procedure. The sample buffer consisted of 4 mL distilled water, 1 mL 0.5 mol/L Tris–HCl, 0.8 mL glycerol, 1.6 mL 10% sodium dodecylsulfate, 0.4 mL 2-mercaptoethanol, and 0.2 mL 0.05% (weight:volume) bromophenol blue. Gels were run for 2 hours at a constant current of 0.2 A (70–100 V) in a 1× Tris–glycine running buffer in a Bio-Rad system (Mini-Protein: catalog number 165-3301). Western blots followed standard procedures, using a Bio-Rad Mini-Transblot apparatus (catalog number 170-3930) and nitrocellulose membranes (0.45-μm pore: Bio-Rad, catalog number 162-0145). After blocking the membranes with 3% fish gelatin or 1% bovine serum albumin in tbs, the recaf bands were evidenced by incubating the membrane with a suitable concentration of anti-recaf antiserum or pure afp biotinylated with Sigma–Aldrich nhs-biotin according to the manufacturers’ instructions. Color development was obtained using diaminobenzidine and H2O2 after the membranes had been incubated with a commercial conjugate (Sigma–Aldrich) of either streptavidin (for the biotinylated afp) or anti-rabbit immunoglobulin labeled with horseradish peroxidase.
The recaf was radioiodinated with Na125I using the chloramine T method 21, with minor modifications. Briefly, 40 μg pure recaf in a volume of 435 μL was mixed with 127 μL 0.4 mol/L sodium phosphate buffer (pH 7.4), to which was then added 37 MBq of Na125I in a volume of 10 μL. Then, 20 μL chloramine T 1 mg/mL in H2O was added, and the mixture was incubated at room temperature for 60 seconds. The reaction was stopped with 20 μL sodium metabisulfite 2.5 mg/mL in phosphate buffer. After 60 seconds, 40 μL 1% Ovalbumin (Sigma–Aldrich) in pbs and 40 μL blue dextran solution were added. The 125I-recaf was then separated from free iodine on a Sephadex G-25 column (Pharmacia, Uppsala, Sweden) made with a disposable 5-mL pipette equilibrated with pbs, pH 7.4. The specific activity of the labeled 125I-recaf ranged from 74 kBq to 370 kBq per microgram of protein (3.7–11.1 kBq/μL).
Circulating levels of carcinoembryonic antigen (cea) and cancer antigen 15-3 (ca15-3) were measured at the Institut für Klinische Chemie, Munich, using the AxSYM system (Abbott Laboratories, Abbott Park, IL, U.S.A.) for cea and the Elecsys system (Hoffmann–La Roche, Nutley, NJ, U.S.A.) for ca15-3.
The recaf determinations were made at the Pacific Biosciences Research Centre facilities in Vancouver, British Columbia.
The test was designed as a solid-phase competitive immunoassay in which a constant amount of 125I-recaf competed with recaf in the serum sample for binding to the anti-recaf antibody immobilized on the plastic plate. The 96-well plates (LockWell MaxiSorp: Nalge Nunc International, Rochester, NY, U.S.A.) were coated overnight, at 4°C, with 100 μL/well of 20 μg/mL rabbit anti-recaf protein A purified immunoglobulin G in 0.1 mol/L carbonate buffer (pH 9.5). All subsequent steps were carried out at room temperature. After being washed 3 times with dH2O, the wells were blocked for 2 hours with 3% fish gelatin (Sigma–Aldrich) in tbs. A mixture of 50 μL serum and 50 μL 125I-recaf at 100 ng/mL was then transferred to the wells and incubated for 2 hours. The wells were washed 3 times with dH2O, each well was separated from the plastic frame, and radioactivity was measured on a gamma counter (ISOdata 20/10: Global Medical Instrumentation, Ramsey, MN, U.S.A.).
Blood was collected and processed according to approved standard protocols. The study included blind samples and open samples (in the latter, the diagnosis was previously known to the person conducting the assay). All samples were collected before treatment was administered; the diagnoses were histologically confirmed before the start of the present study.
In a routine clinical laboratory procedure, blood that had been drawn in sterile tubes without chemicals or in S-Monovette SST tubes (Sarstedt, Nümbrecht, Germany) was allowed to clot and was then centrifuged. Aliquots of serum were stored at −20°C. Before samples were tested for recaf, they were thawed, heated for 30 minutes at 56°C, and supplemented with 0.02% thimerosal.
Levels of recaf had previously been measured in 260 healthy girls and women 13–96 years of age, distributed as follows: <20 years (n = 2), 20–29 years (n = 22), 30–39 years (n = 41), 40–49 years (n = 70), 50–59 years (n = 64), 60–69 years (n = 30), 70–79 years (n = 18), and ≥80 years (n = 13). Linear regression analysis of recaf against age yielded R2 = 0.01 (F = 0.11), indicating that age does not influence the level of circulating recaf. Table i gives the age data for each group.
Descriptive statisticsa for the receptor for alpha-fetoprotein (recaf) in normal, benign, and cancer samples
The three sample sets used in the study were:
Several dilutions of the MCF-7 cell extract were used to create a standard curve calibrated in arbitrary “recaf units” that allowed for the recaf measurements to be normalized from one experiment to another. The dilutions were carried out in 3% fish gelatin–tbs and were processed in the same manner as the serum samples. All sample readings were within the range of the standards. To extrapolate values from the standard curve, we used the Logit/Log function.
The radioimmunoassay design required pure recaf. Figure 1 shows that the recaf preparation used for rabbit immunizations and for radiolabelling has only 1 band with a molecular weight of approximately 62 kDa. That band is recognized by both biotinylated-afp and the rabbit anti-recaf antiserum. The monospecificity of the antiserum was verified against a total cell extract of MCF-7 as shown in lane 5 of Figure 1. The biotinylated-afp also detected a faint 67-kDa band that was absent from the Western blot done with the antiserum. (It is worth noting that the afp receptor has previously been described as a 62/67 kDa doublet found both in soluble form and associated to membranes 22,23.) The rabbit antiserum also inhibited the binding of biotinylated-afp to recaf (data not shown), which indicates that they both recognize the same recaf epitope.
Sodium dodecylsulfate (sds) polyacrylamide gel electrophoresis and Western blot of rabbit antibody to receptor for alpha-fetoprotein (recaf). Lane 1: Molecular weight (MW) markers stained with Coomassie blue. Lane 2: Pure recaf preparation (MW: approximately ...
Ten blind samples distributed within the range of measured recaf values were repeatedly tested to determine the intra- and inter-sample variability of the assay. The intra-sample coefficient of variation was ≤6% and the inter-assay coefficient of variation was <10%.
Comparative distribution of samples from normal subjects, patients with benign breast lesions, and patients with breast cancer for each set of values and for all values combined. The notched box shows the median, the lower and upper quartiles, and the ...
Set 1 (Cancer Stages I and II, Blind Samples): The p value of an independent t-test (assuming unequal variances) comparing normal with cancer samples was 4.78×10−22. When benign and cancer samples were compared, the p value of the t-test was 1.3×10−4.
Figure 3 depicts the receiver operating characteristic (ROC) curves for cea, ca15-3, and recaf when normal samples were compared with samples from cancer patients. For recaf, the area under the curve (AUC) was 0.983. Using a cut-off value of 4.6 K recaf units, the sensitivity was 93%, with 95% specificity. At 95% specificity, the cea sensitivity was 39% (AUC: 0.723) and the ca15-3 sensitivity was 41% (AUC: 0.739).
Receiver operating characteristic curves for the receptor for alpha-fetoprotein (recaf) in samples from cancer patients and from normal subjects [area under the curve (auc): 0.987], for carcinoembryonic antigen (cea, auc: 0.723), and for cancer antigen ...
Increasing the recaf assay cut-off to 7.30 K units to attain 100% specificity, 72% detection of early breast cancers resulted. At 100% specificity, the cea and ca15-3 sensitivities were 32% and 7.3% respectively.
When benign samples were compared with samples from cancer patients (Figure 4), the higher recaf cut-off fared better. At 7.3 K units, the sensitivity was 72%, with 85% specificity (AUC: 0.773). On the same samples, at 85% specificity, the sensitivities of the cea and ca15-3 tests were 34% (AUC: 0.626) and 44% (AUC: 0.685) respectively.
Receiver operating characteristic curves for the receptor for alpha-fetoprotein (recaf) in samples from cancer patients and from patients with benign lesions of the breast [area under the curve (auc): 0.77], for carcinoembryonic antigen (cea) (auc: 0.723), ...
Set 2 (Cancer Stages II and III, Open Samples): Figure 5 shows the recaf ROC curves comparing control and benign samples with samples from cancer patients in Sets 2 and 3. At a cut-off value of 4.61 K recaf units, the sensitivity was 97% and the specificity was 97.5% (AUC: 0.99). When benign and cancer samples were compared using a cut-off of 5.3 K units, the sensitivity was 87%, with 97% specificity (AUC: 0.97).
Receiver operating characteristic curves for the receptor for alpha-fetoprotein (recaf) for (A) Sets 2 and 3 (open samples), and (B) for all 3 sets combined.
Set 3 (Unspecified Cancer Stages, Open Samples): Set 3 included only control and cancer samples. In the ROC analysis, at 4.53 K recaf units, the sensitivity was 89%, with 100% specificity (Figure 5). The AUC was 0.98.
Figure 5 also shows the recaf ROC curves obtained after combining the normal, benign, and cancer samples from all sets.
The results presented here show that a recaf-based serum immunoassay can discriminate, with high sensitivity and specificity, 504 normal subjects and 50 patients with benign breast lesions from 147 patients with breast cancer. More importantly, the assay can detect the early stages of breast cancer with a sensitivity and specificity unattainable to this point with other cancer markers.
Selecting a low cut-off value (4.6 K recaf units) maximizes cancer detection: sensitivity of 93%, with 95% specificity against normal subjects. In the blind group (Set 1), increasing the cut-off to 7.3 K units resulted in 100% specificity against normal subjects, and yet, against early cancers, the sensitivity remained relatively high (72%).
The sensitivity and specificity values in the blind samples (Set 1) were obtained when samples from stages i and ii breast cancer were tested. At those stages, the 5-year survival rates are 87% and 75% compared with 46% and just 13% for stages iii and iv 24. By contrast, the sensitivity reported by an expert panel from the American Society of Clinical Oncology for cea in stage i breast cancer was only 10%; for stage ii, it was 19% (both measured at 95% specificity 25 against normal subjects). In the same study, the sensitivity reported for ca15-3 was 9% in stage i cancer and 19% in stage ii, with a specificity of 95% against normal subjects and a specificity of 80% against benign breast lesions 26. In the present study, the sensitivity exhibited by the cea and ca15-3 tests was higher (39% and 41% respectively, both at 95% specificity). When sera from cancer patients were compared with sera from patients with benign breast lesions, the sensitivities for cea and ca15-3 were also higher than the published data already mentioned; and yet, the performance of the recaf assay was significantly better than either one of those two markers.
Using a cut-off value of 7.3 K units, the discrimination of positive cases among benign sera in the blind samples of Set 1 was 15%, which is slightly less than the 20% reported for ca15-3 25. In two thirds of benign samples, testing showed levels of less than 6 K recaf units.
The results from Sets 2 and 3 (open samples) were consistent with those from the blind group (Set 1), thus significantly expanding the number of samples.
It is unclear why some benign lesions are recaf-positive. It is common knowledge that, in general, cancer markers detect a certain percentage of benign lesions. Several explanations are possible:
Future work on the biology of recaf might explain why some benign breast lesions test positive and might perhaps provide insight into how to better interpret the results of the recaf test.
5. CONFLICT OF INTEREST DISCLOSURES
RM and JGT receive remuneration from the company that owns the intellectual property rights for use of the recaf marker. PS has no financial conflicts of interest to disclose.