|Prostate cancer cell phenotypes based on AGR2 and CD10 expression.|
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|PMID: 23348903 Owner: NLM Status: MEDLINE|
|The combination of expression patterns of AGR2 (anterior gradient 2) and CD10 by prostate cancer provided four phenotypes that correlated with clinical outcome. Based on immunophenotyping, CD10(low)AGR2(high), CD10(high)AGR2(high), CD10(low)AGR2(low), and CD10(high)AGR2(low) were distinguished. AGR2(+) tumors were associated with longer recurrence-free survival and CD10(+) tumors with shorter recurrence-free survival. In high-stage cases, the CD10(low)AGR2(high) phenotype was associated with a ninefold higher recurrence-free survival than the CD10(high)AGR2(low) phenotype. The CD10(high)AGR2(high) and CD10(low)AGR2(low) phenotypes were intermediate. The CD10(high)AGR2(low) phenotype was most frequent in high-grade primary tumors. Conversely, bone and other soft tissue metastases, and derivative xenografts, expressed more AGR2 and less CD10. AGR2 protein was readily detected in tumor metastases. The CD10(high)AGR2(low) phenotype in primary tumors is predictive of poor outcome; however, the CD10(low)AGR2(high) phenotype is more common in metastases. It appears that AGR2 has a protective function in primary tumors but may have a role in the distal spread of tumor cells.|
|Melissa E Ho; Sue-Ing Quek; Lawrence D True; Colm Morrissey; Eva Corey; Robert L Vessella; Ruth Dumpit; Peter S Nelson; Erin L Maresh; Vei Mah; Mohammed Alavi; Sara R Kim; Lora Bagryanova; Steve Horvath; David Chia; Lee Goodglick; Alvin Y Liu|
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|Type: Journal Article; Research Support, N.I.H., Extramural Date: 2013-01-25|
|Title: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc Volume: 26 ISSN: 1530-0285 ISO Abbreviation: Mod. Pathol. Publication Date: 2013 Jun|
|Created Date: 2013-06-03 Completed Date: 2014-01-13 Revised Date: 2014-08-20|
Medline Journal Info:
|Nlm Unique ID: 8806605 Medline TA: Mod Pathol Country: United States|
|Languages: eng Pagination: 849-59 Citation Subset: IM|
|APA/MLA Format Download EndNote Download BibTex|
Bone Neoplasms / genetics, metabolism*, mortality, secondary
Carcinoma / genetics, metabolism*, mortality, secondary
Mice, Inbred BALB C
Neoplasm Recurrence, Local
Neprilysin / metabolism*
Proportional Hazards Models
Prostatic Neoplasms / genetics, metabolism*, mortality, pathology
Proteins / metabolism*
Tissue Array Analysis
Tumor Markers, Biological / metabolism*
|CA111244/CA/NCI NIH HHS; CA86366/CA/NCI NIH HHS; P30 CA016042/CA/NCI NIH HHS; P50 CA097186/CA/NCI NIH HHS; P50 CA097186/CA/NCI NIH HHS; U01 CA111244/CA/NCI NIH HHS|
|0/Proteins; 0/Tumor Markers, Biological; EC 126.96.36.199/Neprilysin; EC 188.8.131.52/AGR2 protein, human|
Journal ID (nlm-journal-id): 8806605
Journal ID (pubmed-jr-id): 6644
Journal ID (nlm-ta): Mod Pathol
Journal ID (iso-abbrev): Mod. Pathol.
nihms-submitted publication date: Day: 28 Month: 11 Year: 2012
Electronic publication date: Day: 25 Month: 1 Year: 2013
Print publication date: Month: 6 Year: 2013
pmc-release publication date: Day: 01 Month: 12 Year: 2013
Volume: 26 Issue: 6
First Page: 849 Last Page: 859
PubMed Id: 23348903
|Prostate cancer cell phenotypes based on AGR2 and CD10 expression|
|Melissa E. Ho12|
|Lawrence D. True3|
|Robert L. Vessella14|
|Peter S. Nelson5|
|Erin L. Maresh6|
|Sara R. Kim6|
|Alvin Y. Liu12|
1Department of Urology, University of Washington, Seattle, Washington, USA
2Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington, USA
3Department of Pathology, University of Washington, Seattle, Washington, USA
4Puget Sound VA Medical Center, Seattle, Washington, USA
5Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA
6Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, California, USA
7Department of Biostatistics, David Geffen School of Medicine, University of California, Los Angeles, California, USA
8Jonsson Comprehensive Cancer Center, David Geffen School of Medicine, University of California, Los Angeles, California, USA
|Correspondence: Correspondence: Dr. AY Liu, Ph.D., Department of Urology, University of Washington, Box 358056, 850 Republican Street, Seattle, WA 98195-6100, USA. email@example.com
Although prostate cancer is the most frequent cancer in men, only a minority of affected men die of the disease. Serum levels of prostate-specific antigen (PSA/KLK3) are widely used to screen men for prostate cancer. However, with a false positive rate of nearly 70% many unnecessary biopsies are being performed.1 Prostate cancer is histologically characterized by the Gleason grading system. Cases with predominantly pattern 3 tumor predict long-term survival, with or without active intervention. Cases with a pattern 4 or pattern 5 component are associated with poorer outcomes. For many patients, PSA level and Gleason score, in addition to post-surgery clinical staging, show relatively good performance in disease prognosis (the Partin nomogram - http://urology.jhu.edu/prostate/partintables.php).2 There remain many cases where the known predictors fail. Thus, not only are informative biomarkers needed to detect early stage cancer with good confidence but also, more importantly, to identify patients whose cancer requires treatment. An early and reliable differentiation between patients with good vs. poor prognosis cancer could substantially reduce unnecessary morbidity-generating interventions for long-term survivors. Molecular signatures that provide objective classification will eventually enable such categorization of patients. In addition, such a categorization would ideally be made using either small biopsies or biofluids such as urine or blood.
Prostate cancer cells differentially express AGR2 (anterior gradient 2) and CD10/MME (membrane metallo-endopeptidase). AGR2 encodes a 19-kDa secreted protein, MME encodes a 100-kDa cell surface membrane protein. AGR2 expression is increased in prostate cancer cells (and cells of high-grade prostatic intraepithelial neoplasia, PIN) compared to the normal counterpart luminal epithelial cells.3-6 CD10, in contrast, is decreased in cancer cells, although about 30% of tumors express CD10.7-9 Tumors with CD10+ cancer cells tend to be more frequent in higher Gleason score cancers, and CD10+ cancer cells predominate in regional lymph node metastases.8-10 Conversely, AGR2+ tumors predominate in lower Gleason score cancers, and cancer cells of Gleason patterns 4 and 5 tend to express lower levels of AGR2.5,6
Expression of CD10 by prostate cancer correlates with poor disease outcome and lower rates of patient survival.9-11 In addition, cytoplasmic rather than membraneous localization of the CD10 protein in tumor cells is associated with poor outcome.11 This finding could be attributed to the association of CD10 with cytoplasmic heat shock proteins such HSP27 (HSPB1) in prostate cancer cells; CD10+ luminal cells do not express HSP27.12 In contrast, prostate cancer expression of AGR2 correlates with longer patient survival.5 Could differential expression by cancer cells of CD10 and AGR2 provide more precise prognostic information?
In this study, expression of AGR2 and CD10 by prostate cancer was probed in a tissue microarray of over 200 radical prostatectomy cases in which outcomes were known. Immunohistochemistry allowed us to identify different cancer cell phenotypes based on expression levels of these two markers. AGR2 and CD10 expression was further probed in tissue microarrays of bone and soft tissue metastases, and of tumor xenografts, with the expectation that they might reveal phenotypes linked to poor outcomes.
This study is approved by our institutional review boards.
The tissue microarrays of primary tumors and prostate cancer metastasis, LuCaP prostate cancer xenografts were constructed with cores of 0.6 mm and 1 mm in diameter, respectively, from blocks of formalin-fixed, paraffin-embedded tissues. Three tissue microarrays were used: 1) primary prostate tumors (UCLA TMA) constructed from 246 randomly selected hormone-naïve cases treated by surgery with three morphologically representative biopsies of each tumor, plus matching benign tissue and available in situ neoplastic lesions (PIN); biochemical recurrence was the indication used for treatment failure;5,13 2) prostate cancer metastases (UW TMA22) procured from donor autopsies (i.e., representative of late-stage disease) with n=248 cores from 124 different sites of 23 patients; 3) the LuCaP series of prostate cancer xenografts, n=24, serially passaged in immune compromised mice (UW TMA46).
For analysis, 6 μm-thin sections were cut from each array block. Following deparaffinization and antigen retrieval (by boiling in 0.01 M citrate buffer for 25 min), endogenous peroxidase activity was quenched and the sections treated with 5% goat-horse-chicken serum. Slides were incubated overnight with either rabbit polyclonal AGR2 antibody (ab43043, abcam, Cambridge, MA) at 1:30 or mouse monoclonal CD10 antibody (clone 56C6, Lab Vision, Fremont, CA) at 1:30 in 0.1% bovine serum albumin-phosphate buffered saline. Specific staining was detected by applying anti-rabbit or anti-mouse horseradish peroxidase-conjugated secondary antibody and avidin-biotin complex followed by diaminobenzidine (Vector ABC, Burlingame, CA). As negative controls, tissue was incubated with concentration-matched non-immune IgG. Frozen sections were also prepared from OCT tissue blocks, and were stained with either monoclonal anti-AGR2 (clone P1G4, IgG1)14 at 1:30, or anti-CD10 (clone HI10a, IgG1, BD Bioscience, San Jose, CA) at 1:30.
The percentage of glandular cell staining was scored from 0-100% and the intensity of staining was rated from 0 (absent immunoreactivity) to 3 (intense). An integrated measure of expression for frequency and intensity of staining was calculated using the following formula: [3(%x)+2(%y)+1(%z)]/100, where x, y, and z represented the percentage of cells staining at intensity 3, 2, and 1, respectively. For outcomes analysis, a mean pooled value for each case was calculated. Protein expression was correlated with disease outcome, clinicopathological variables,13 and recurrence following radical prostatectomy.
Briefly, non-parametric two-group and multi-group comparisons were carried out using Mann-Whitney and Kruskal-Wallis tests. Correlations were calculated using Spearman Correlation. Patients were dichotomized at an optimal cutpoint, and recurrence-free survival curves were visualized using the Kaplan-Meier method with the difference between outcome distributions assessed by the log-rank test. The Cox proportional hazards model was used to test the statistical significance of predictors in both a univariate and a multivariate setting. All statistical analyses were performed with StatView Version 5.0 (SAS Institute) or with the freely available software package, R (http://www.r-project.org).
Tissue microarray immunohistochemistry was similarly performed for the arrays containing the LuCaP xenografts and metastases.
The xenografts were maintained and propagated in Balb/c nu/nu intact male mice, and the castration-resistant variants were developed from parental tumors on regrowth after castration. These were maintained and propagated in castrated B17 Fox Chase SCID male mice (Charles River, Wilmington, MA).15 The origin and characteristics of all serially passaged xenografts were described in ref. 16,17. None of these xenografts could be grown in vitro. Xenografts were harvested at 100 mg size, frozen for storage, and each was processed for RNA isolation using STAT60 (Tel-Test, Friendswood, TX).
Metastasis specimens were collected from rapid autopsies of patients who died from metastatic prostate cancer performed under the aegis of the IRB-approved Prostate Cancer Donor Program at the University of Washington Medical Center.18 Within 4 h of death, samples of all gross tumors and bone metastases were obtained under sterile conditions. Each specimen was assigned a unique laboratory research number and rapidly frozen or formalin fixed (bone metastases were decalcified in formic acid) and paraffin embedded. RNA was similarly prepared from frozen specimens using STAT60.
For array analysis, tumor (xenograft and metastasis) RNA was amplified one round and hybridized to Agilent 44K whole human genome expression oligonucleotide microarrays (Agilent Technologies, Santa Clara, CA). Probe labeling and hybridization was performed following the Agilent protocol, and fluorescent array images were collected using the Agilent DNA microarray scanner G2565BA. Agilent Feature Extraction software was used to grid, extract, and normalize data as reported in ref. 19.
BD Falcon Flexible (Franklin Lakes, NJ) plates were coated with purified monoclonal antibody P1G4 (1:1,000) in phosphate buffered saline overnight at 4°, rinsed 3x with phosphate buffered saline-0.05% Tween, blocked with 1% heat-denatured bovine serum albumin-phosphate buffered saline. Cell-free tissue digestion media and spent cancer cell line culture media samples were added for incubation at 4° overnight. Monoclonal antibody P3A5 (IgG2a, 1:1,000)14 was then added for 1 h at room temperature. For detection, horse radish peroxidase-conjugated anti-mouse IgG2a was used for 30 min at room temperature. 2,2′-Azinobis[3-ethylbenzothiazoline-6-sulfonic acid]-diammonium salt (KPL/Fisher, Belgium) was the chromogenic reagent for measurement at λ=405 nm. A standard curve was obtained by using recombinant AGR2 (GenWay Biotech, San Diego, CA) as described.14
In a majority of prostate tumors, AGR2 expression was increased and CD10 expression decreased relative to luminal epithelial cells of benign glands (Figure 1). Thus, cancer cells were CD10−AGR2+ and luminal cells were CD10+AGR2−. In the example shown, the adjacent tumor and benign glands were clearly distinguished by phenotyping with these two markers. Faint AGR2 staining of the stroma surrounding the cancer glands could indicate that AGR2 was secreted. No such staining feature was seen for CD26 (DPP4), a cell surface antigen on luminal and cancer cells previously used in cell sorting for transcriptome analysis.4 This pattern of AGR2 increase and CD10 decrease was also found in the glands of PIN present in this tumor tissue specimen (Figure 1). In cancer cells, AGR2 staining intensity and DNA array expression values for AGR2 probesets4,14 indicated moderately abundant levels of the protein and the transcript.
We have previously identified a trend of lower AGR2 expression in higher Gleason grades,5 and a trend of more CD10-positive tumor cells in higher Gleason grades.8,9 In the present study, analysis of AGR2 and CD10 expression showed a correlation between the CD10lowAGR2high tumor phenotype and greater recurrence-free survival in high-stage patients (III/IV) as shown in Figure 2 [while almost all low-stage (I/II) patients were cured of their disease by surgery]. In contrast, patients with CD10highAGR2low tumors had the lowest recurrence-free rate. At about 60 months post-surgery, >80% of the CD10lowAGR2high patients showed no recurrence, whereas only <30% of the CD10highAGR2low patients did (P=0.0247). Patients with CD10highAGR2high and CD10lowAGR2low tumors showed intermediate rates. Thus, for high-stage patients whose overall survival was relatively poor, a small group of men with CD10lowAGR2high tumors still experienced a favorable outcome.
High CD10 and low AGR2 expression might be the basis of high disease stage as indicated by the relative percentages of these phenotypes. There were six cases of CD10lowAGR2high (10%), 13 cases of CD10highAGR2high (21%), 8 cases of CD10lowAGR2low (13%), and 36 cases of CD10highAGR2low (57%) in this patient subgrouping. Over half of the high-stage patients contained CD10highAGR2low cancer cells in their tumor, whereas only 10% contained CD10lowAGR2high cancer cells in their tumor. Examples of specimens staining for CD10 and AGR2 are shown in Figure 3 for the four phenotypes CD10+AGR2+, CD10−AGR2+, CD10+AGR2−, CD10−AGR2−. Note the first three cases all showed glandular differentiation (i.e., Gleason pattern 3) yet the outcome would be different due to their different AGR2/CD10 phenotyping.
Table 1 shows the dataset of the tissue microarray cases in pairwise comparison (A grouping vs. B grouping). cRR was the current hazard ratio between individual A and B groupings where cRR<1 if A showed higher survival and >1 if B showed higher survival. In row 1, the CD10lowAGR2high group showed higher survival by 5-fold than the CD10lowAGR2low group. This indicated that tumor expression of AGR2 had perhaps a protective effect. In row 5, the CD10highAGR2low group showed lower survival by 9-fold than the CD10lowAGR2high group with the largest observed difference. This indicated that tumor expression of CD10 had a deleterious effect.
Based on the above findings in primary tumors, one would expect the CD10highAGR2low phenotype to be predominant in metastases of distal organs. Figure 4 shows immunoreactivity of selected bone/soft tissue metastases. Examples of AGR2/CD10 phenotypes included CD10lowAGR2high 05-116E2 liver, CD10lowAGR2high 05-116F2 lung, CD10−AGR2high 06-047H2 iliac lymph node, CD10−AGR2− 05-144G1 retroperitoneal lymph node, CD10−AGR2− 03-192A3 liver, CD10−AGR2+ 99-064DD1 L4 vertebra, CD10−AGR2+ 05-214DD4 sacrum, CD10lowAGR2high 05-011F3 liver, CD10−AGR2+ 04-050DD3 sacrum, CD10−AGR2− 03-082H2 liver. The tumors showed a range of expression levels (hence the “high” or “low” indication) and the staining was cytoplasmic for AGR2. Of these, only 3/10 showed no AGR2 expression while 7/10 showed no CD10 expression. The AGR2-negative tumors were all small cell carcinoma: 05-144G1, 03-192A3, 03-082H2; plus 05-144EE1 shown in Figure 5. The AGR2 pattern in metastases was corroborated by DNA microarray analysis (Figure 5). For example, the stronger overall AGR2 staining of 00-140FF than 07-050EE1 was reflected in the DNA microarray signal values. CD10 expression was also confirmed, and the small cell carcinoma samples showed low values for CD10 (05-144EE2, a sister sampling to 05-144EE1, Figure 5). Thus, the predominant cancer cell phenotype in distal metastasis was not CD10highAGR2low but rather CD10low/−AGR2high. Note that the metastasis samples were obtained from patients likely treated by androgen ablation and other types of therapy, whereas the primary cancer samples were from patients treated by surgery only.
Testing of tissue collagenase digestion media by ELISA further supported the AGR2 data. For reference, AGR2 protein in the culture media of cell lines C4-2, C4-2B, CL1 and PC3 was used (Figure 6). C4-2 was negative for AGR2; a small amount was detected in C4-2B; high amounts in PC3 and CL1.14 For multiple metastasis specimens, AGR2 was detected (Figure 6). The specimens were obtained from both donor autopsies and surgical procedures (98-378 bone and 00-061 node).
Figure 7 shows the RNA expression levels of AGR2 and CD10 in cancer cell lines and xenografts. Luminal epithelial cells (L), Gleason pattern 3 (G3) and Gleason pattern 4 (G4) cancer cells of primary tumors (ref. 4) were also shown. C4-2 and CL1 were both derived from LNCaP by androgen manipulation. LuCaP 35 is similar to LNCaP in gene expression; both were established from positive lymph nodes.20 LuCaP 49, characterized by minimal AGR2 and CD10 expression, is representative of small cell carcinoma.21 Among them, these phenotypes were found – CD10−AGR2+ G3 cancer, CL1, PC3; CD10highAGR2low LuCaP 35; CD10−AGR2low G4 cancer; CD10+AGR2− LNCaP, C4-2; CD10−AGR2− DU145, LuCaP 49. It appeared that cancer cell lines considered to be more aggressive, PC3 and CL1, showed increased AGR2 and decreased CD10 expression. This was not the case for G3 vs. G4 cells of primary tumors where lower levels of AGR2 were found in the potentially more aggressive G4 cells.
Figure 8 shows immunostains of LuCaP xenografts (Table 2) harvested from subcutaneous tumors passaged in mice. The AGR2/CD10 phenotypes were: CD10lowAGR2high LuCaP 23.12 (established from a liver metastasis), LuCaP 105 (rib); CD10highAGR2low LuCaP 141 (transurethral resection of the prostate), LuCaP 86.2 (bladder); CD10lowAGR2low LuCaP 81 (lymph node); CD10−AGR2− LuCaP 145.1 (liver). LuCaP 145.1 was representative of small cell carcinoma, and like LuCaP 49 (and LuCaP 93, LuCaP 145.2), was negative for both markers. LuCaP 141, established from a surgical specimen of primary cancer, and LuCaP 86.2, from a resected bladder metastasis, expressed CD10. Protein expression was corroborated by DNA microarray analysis of these xenografts (Figure 9).
LuCaP 35CR, LuCaP 96CR, LuCaP 23.1CR (CR=castration resistant) provided a means to examine the effect of androgen ablation on the expression of AGR2 and CD10. Based on immunostaining, the phenotypes were CD10−AGR2− for LuCaP 23.1, CD10highAGR2low for LuCaP 35, CD10lowAGR2high for LuCaP 96. It is unclear why the DNA microarray results for LuCaP 23.1 and LuCaP 96 were discordant with immunostaining (Figure 9). Androgen removal appeared to reduce overall staining of CD10 in LuCaP 96CR (Figure 10). DNA array analysis also showed a decrease in LuCaP 96CR (Figure 9). For AGR2, some weak focal staining in LuCaP 23.1CR, and strong staining between tumor cells in LuCaP 96CR was detected (Figure 10). These results were akin to that in the derivation of CD10+AGR2− C4-2 from CD10+AGR2− LNCaP in castrated animals. Since the LuCaP tumors cannot be cultured in vitro, a similar pathway (i.e., long-term growth in androgen-free media) to obtain CD10−AGR2+ CL1 from LNCaP could not be duplicated.
AGR2 and CD10 are both biomarkers for prostate cancer. AGR2 expression is lower in cancer cells of higher grades whereas CD10-positive cancer cells are more frequent in higher grade cancers. A small subset of tumors with similar Gleason pattern show differential AGR2/CD10 expression, therefore, AGR2/CD10 phenotyping would perhaps be more useful than Gleason scoring in predicting outcome. AGR2 appears to be protective while CD10 imparts a more aggressive potential in prostate cancer. Thus, even for high-stage patients where overall survival is poor, tumors showing high AGR2 and low CD10 expression would still predict a better outcome. While both AGR2 and CD10 are independently prognostic, in combination, three phenotypes define recurrence probability from low to high: CD10lowAGR2high < CD10highAGR2high = CD10lowAGR2low < CD10highAGR2low. The precise molecular functioning of the two proteins in cancer cells is unknown. Note the luminal cell CD10+AGR2− phenotype corresponds to the aggressive CD10highAGR2low cancer type. The action of these gene products are likely dependent on cell context. Similarly, although G3 cancer and CL1 shared a common phenotype in AGR2 and CD10, their overall gene expression is very different.20
The expression pattern of AGR2 and CD10 in distal metastases of the bone and soft tissues appears at odds with that in primary tumors where potential of cancer spread is correlated with Gleason grade. The majority of these metastases are typed CD10lowAGR2high whereas this phenotype predominates in Gleason 3. Instead, the CD10highAGR2low phenotype in primary tumors is correlated with poor outcome. Most regional lymph node metastases contain CD10+AGR2−/+ tumor cells. For example, CD10+AGR2− LNCaP and CD10+AGR2+ LuCaP 35 are both derived from node metastasis. Outside their metastasis potential, the transcriptomes of LNCaP and LuCaP 35 are similar to that of CD10+AGR2− luminal cells and CD10−AGR2+ G3 cancer cells.20 Additionally, LuCaP 86.2, established from a surgically resected bladder metastasis (representative of local spread), is CD10high. This suggests that CD10+ tumor cells are more likely to escape the prostate than CD10− ones. For distal spread, the functional role of AGR2 becomes more important whereas that of CD10 becomes less important. This hypothesis could explain the expression pattern seen in bone and other organ metastases, which is in line with the experimental data showing AGR2 promoted tumor cell growth and dissemination.22-26 What, then, could cause the phenotypic change to CD10−AGR2+ from escaped CD10+AGR2− tumor cells? One possible mechanism involves physiological stress such as serum depletion or oxygen starvation on cancer cell AGR2 expression.27 Hormone ablation is a physiological stress for prostate cancer cells. The LNCaP cell line was grown in androgen-free media to obtain the androgen independent variant CL1.28 CL1 expresses AGR2 at a high level. LNCaP was also grown in castrated mice with human bone stromal cells to obtain C4-2, and C4-2 was further selected for growth in bone to obtain C4-2B.29 While C4-2 remains CD10+AGR2−, C4-2B produces a small amount of AGR2. PC3, established from a bone metastasis,30 is AGR2+. With the gain of AGR2 expression, the CL1 cells have also lost CD10 expression.31 In the castration resistant LuCaP variants, some weak staining of AGR2 is present in LuCaP 23.1CR vs. complete absent staining in LuCaP 23.1; a decrease in overall CD10 staining is seen in LuCaP 96CR vs. LuCaP 96. This complex expression pattern of CD10 and AGR2 in prostate cancer could explain discrepant conclusions reported in the literature regarding their prognostic value: CD10 expression was correlated with better outcome;7 AGR2 expression was correlated with poorer outcome.32 A similar situation may exist for AGR2 in breast cancer where expression is correlated with poor survival by one study33vs. that with better survival by another.34 In the latter case, AGR2 expression is associated breast cancer differentiation and lower tumor grade as in prostate cancer.
Our working hypothesis is that CD10 and AGR2 have opposing functions in prostate cancer cells. Luminal CD10 expression is lost and AGR2 expression is gained early in cancer development. Certain cancer cells regain CD10 expression (or retain luminal CD10 expression) with or without decrease in AGR2 expression in progression from low to high Gleason grade. CD10 allows the cancer cells to escape the prostate to regional lymph nodes and proximal organs like the bladder. In order for distal spread to organs like bone, the cancer cells require functional AGR2. This hypothesis is supported by the result showing that a surgically removed bone lesion, specimen 98-378, was AGR2 positive, and by the fact that CL1 cells are highly metastatic in mice whereas LNCaP cells are not.28 The LNCaP to CL1 pathway suggests that AGR2 expression could be triggered by a physiological stress such as androgen ablation used in the treatment of post-operative patients with rising PSA.
In summary, the prostate cancer biomarkers, AGR2 and CD10, can be used in combination to stratify prostate cancer patients for clinical outcome. Patients with CD10highAGR2low tumors would appear to fare worse than those with CD10lowAGR2high tumors. However, cancer cells in distal metastases of advanced disease are CD10lowAGR2high.
FN2Disclosure/conflict of interest
The authors declare no conflict of interest.
The research was supported by the NCI Early Detection Research Network (EDRN) grants CA111244 (AYL), CA86366 (DC, LG) and the Pacific Northwest SPORE P50 CA097186 (LDT, CM, EC, RLV, PSN). We thank the patients, families, and clinicians Celestia Higano, Bruce Montgomery, and Martine Roudier in the Rapid Autopsy Program at University of Washington for making available the study material, and Adeline Chen for performing immunostaining.
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Keywords: Prostate cancer, AGR2, CD10, cancer cell phenotypes, patient stratification, bone and soft tissue metastases, xenografts.
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