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Monocarboxylate transporter 4 (MCT4) and CD147 overexpression is associated with poor prognosis in prostate cancer
© Pértega-Gomes et al; licensee BioMed Central Ltd. 2011
Received: 12 February 2011
Accepted: 25 July 2011
Published: 25 July 2011
Monocarboxylate transporters (MCTs) are transmembrane proteins involved in the transport of monocarboxylates across the plasma membrane, which appear to play an important role in solid tumours, however the role of MCTs in prostate cancer is largely unknown. The aim of the present work was to evaluate the clinico-pathological value of monocarboxylate transporters (MCTs) expression, namely MCT1, MCT2 and MCT4, together with CD147 and gp70 as MCT1/4 and MCT2 chaperones, respectively, in prostate carcinoma.
Prostate tissues were obtained from 171 patients, who performed radical prostatectomy and 14 patients who performed cystoprostatectomy. Samples and clinico-pathological data were retrieved and organized into tissue microarray (TMAs) blocks. Protein expression was evaluated by immunohistochemistry in neoplastic (n = 171), adjacent non-neoplastic tissues (n = 135), PIN lesions (n = 40) and normal prostatic tissue (n = 14). Protein expression was correlated with patients' clinicopathologic characteristics.
In the present study, a significant increase of MCT2 and MCT4 expression in the cytoplasm of tumour cells and a significant decrease in both MCT1 and CD147 expression in prostate tumour cells was observed when compared to normal tissue. All MCT isoforms and CD147 were expressed in PIN lesions. Importantly, for MCT2 and MCT4 the expression levels in PIN lesions were between normal and tumour tissue, which might indicate a role for these MCTs in the malignant transformation. Associations were found between MCT1, MCT4 and CD147 expressions and poor prognosis markers; importantly MCT4 and CD147 overexpression correlated with higher PSA levels, Gleason score and pT stage, as well as with perineural invasion and biochemical recurrence.
Our data provides novel evidence for the involvement of MCTs in prostate cancer. According to our results, we consider that MCT2 should be further explored as tumour marker and both MCT4 and CD147 as markers of poor prognosis in prostate cancer.
Increased glucose consumption is a hallmark of malignant cells, which is responsible for energy production from glycolysis . Most malignancies rely on this pathway for rapid proliferation even in the presence of oxygen, leading to production of large amounts of acids, mainly lactic acid [1, 2]. Consequently, the high glycolytic phenotype induces an acidic tumour environment, which is associated with the increase of several malignant features including cellular migration, invasion and metastisation .
In order to prevent cell death by cellular acidosis, tumour cells increase proton efflux through pH regulators such as proton-pumps, sodium-proton exchangers, bicarbonate transporters and monocarboxylate transporters (MCTs) . MCTs are proteins that facilitate the transmembrane transport of short-chain fatty acids, such as pyruvate and lactate, coupled with a proton. In glycolytic tumours, they promote the efflux of lactic acid, constituting important players in the maintenance of tumour intracellular pH, as well as in the maintenance of the high rates of glycolysis [4, 5]. Therefore, MCTs play a central role in tumour metabolism and, as a result, constitute attractive targets in cancer therapy which have not been explored yet.
We and others have shown evidence for the upregulation of MCTs in several solid tumours, such as colorectal carcinomas , uterine cervix carcinomas , melanomas , breast carcinomas [9, 10] and lung tumours . However, in prostate carcinoma, the role of MCTs is largely unknown. To the best of our knowledge, we were the first to report MCT expression in prostate cancer [12, 13], however, there is a recent study  evaluating the role of MCTs in prostate drug resistance and progression but this study does not evaluate neither MCT isoform 2 (MCT2) nor gp70, its known chaperone.
MCT expression appears to be influenced by altered physiologic conditions, however the underlying molecular events involved in MCT regulation are still poorly understood. Recently, it was demonstrated that proper expression and activity of MCT1 and MCT4 requires co-expression of CD147, also known as EMMPRIN or basigin [15–17]. On the other hand, in vitro studies showed that maturation and cell surface expression of CD147 is also dependent on MCT1 and MCT4 expressions [18, 19]. MCT2 expression and activity depends on a different chaperone known as gp70.
CD147 alone has already been described as a key element in oncogenesis by stimulating the synthesis of several matrix metalloproteinases, leading to enhanced tumour cell invasion [20, 21]. This protein is described to be up-regulated in tumours, including prostate cancer, where it has been identified as an unfavourable prognosis marker [22–25]. However, the role of CD147/MCT co-expression in prostate cancer is far from understood.
The aim of the present study was to assess the role of MCTs in prostate cancer, by comparing the immunohistochemical expression of the MCT isoforms 1, 2 and 4, along with CD147 and gp70, in normal prostatic tissue, adjacent non-neoplastic tissue, PIN lesions and neoplastic tissues in a large series of prostate samples organized into tissue microarrays (TMAs), and evaluating their clinico-pathological value.
Case selection and TMA construction
Prostate tissues were obtained from 171 patients with a median age of 64 years old (range 46-74), who performed radical prostatectomy between 1993 and 2003. Samples and clinico-pathological data were retrieved from the files of the Department of Pathology, Centro Hospitalar do Porto and Centro Hospitalar do Alto Ave-Guimarães, and organized into 13 tissue microarray blocks (TMAs).
Prior to TMA construction, hematoxylin and eosin (H&E) tumour sections of each specimen of radical prostatectomy were re-assessed using the 2005 modified Gleason and 2010 p TNM AJCC classification [26, 27]. Representative areas of adjacent non-neoplastic prostate tissue, PIN lesions and prostate cancer were selected. Adjacent non-neoplastic tissue samples and PIN lesions were selected from the peripheral zone of prostate were cancer develops. Each case was represented in the TMA by three cores (1 mm diameter) with 0.8 mm from core centre to core centre, and precisely deposited into a recipient paraffin block, using a TMA workstation (TMA builder, Beecher Instruments Inc. Technology). 4 μm tissue sections were used for immunohistochemistry (IHC) and H&E-stained section from each TMA block was reviewed to confirm the presence of morphological representative areas of the original tissues.
Normal prostate tissue was obtained from cystoprostatectomy cases and immunohistochemical expression was performed in the entire section of the fragments.
MCT and CD147 immunohistochemistry
IHC for MCTs was performed according to avidin-biotin-peroxidase complex principle (R.T.U. Vectastain Elite ABC Kit [Universal], Vector Laboratories, Burlingame, CA), with the primary antibodies for MCT1 (AB3538P, Chemicon International, Temecula, CA), MCT2 (sc-14926, Santa Cruz Biotechnology, Santa Cruz, CA) and MCT4 (AB3316P, Chemicon International, Temecula, CA), diluted 1:200, as previously described [6, 7, 9, 10].
CD147 and gp70 IHC was performed according to the same principle (Ultravision Detection System Antipolyvalent, horseradish peroxidase; Lab Vision Corporation), with the primary antibody diluted 1:750, as previously described [9, 10] for CD147 (18-7344, ZYMED Laboratories Inc., South San Francisco, CA) and diluted 1:100 for gp70 (HPA017740, Atlas Antibodies).
Negative controls were performed with appropriate serum controls for the primary antibodies (X0907 and N1699, Dako, Carpinteria, CA). Normal colon, kidney and skeletal muscle tissue were used as positive controls for MCT1, MCT2 and MCT4, respectively, cervical squamous carcinoma for CD147 and seminal vesicle for gp70. Tissue sections were counterstained with hematoxylin.
Immunoreaction in TMA sections was evaluated for cytoplasmic and/or plasma membrane staining. Shortly, sections were scored semi-quantitatively as follows: 0: 0% of immunoreactive cells; 1: < 5% of immunoreactive cells; 2: 5-50% of immunoreactive cells and 3: > 50% of immunoreactive cells. Also, intensity of staining was scored semi-quantitatively as follows: 0: negative; 1: weak; 2: moderate and 3: strong. The final score was defined as the sum of both parameters (extension and intensity), and grouped as negative (scores 0-3) and positive (scores 4-6). Discordant results in different cores of the same case were scored as follows: average of extension plus highest intensity score. Immunohistochemical evaluation was performed by two independent and experienced pathologists (JRV, PM), who were blind to the clinico-pathological data of the patients. Discordant results were discussed in a double-head microscope. Since staining was different among the positive cases, to further clarify the significance of the immunoexpression of MCTs and CD147 in prostate carcinoma, we categorized the cases in two groups: intermediate score group (ISG, score 4) and high score group (HSG, scores 5-6).
Statistical analysis was performed using the SPSS statistical software (version 17.0, SPSS Inc., Chicago, IL, USA). All comparisons were examined for statistical significance using Pearson's chisquare (χ 2) test, being the threshold for significance p < 0.05.
The work has been approved by DEFI (Departamento de Ensino Formação e Investigação) Ethics Committee of Centro Hospitalar do Porto ref. no. 017/08(010-DEFI/015-CES).
MCT, CD147 and gp70 expressions in prostate tissues
Distribution of positive final immunohistochemical score of monocarboxylate transporters (MCTs) and CD147 in adjacent non-tumoural (NT) and tumour tissue (T) of prostate samples
Association between MCT1, MCT2, MCT4 and CD147 expressions in prostate tumours
Associations between MCTs and CD147 expressions and the clinic-pathological data
Correlations between monocarboxylate transporters (MCTs) and CD147 expressions in prostate tumour samples and clinico-pathological data
Prostate cancer remains a major concern in public health, being one of the most prevalent tumours and the second leading cause of cancer death in men . Thus, it is important to elucidate its biology in order to find new markers and more efficient treatments.
Experimental evidence points at MCTs as potential targets for cancer therapy [29, 30], however, the role of these membrane proteins in prostate cancer is poorly understood. Thus, the present work is an attempt to shed light into the involvement of MCTs in prostate cancer. With this purpose, we analysed the expressions of MCT1, MCT2, MCT4, CD147 and gp70 in a series of prostate samples, including normal, adjacent non-neoplastic, PIN lesions and neoplastic tissues.
MCT1, MCT2, MCT4 and CD147 are differentially expressed in non-neoplastic, PIN lesions and neoplastic prostate tissues
In the present study, a general decrease in MCT1 and CD147 levels from normal prostate tissue to PIN lesions and prostate carcinoma was observed. Since their expression in normal prostate epithelium is high, it appears that they have an important role in normal tissue and are downregulated in prostate cancer cells, where other adaptive mechanisms may be activated. Importantly, there was an increase in both MCT2 and MCT4 expressions from normal to PIN lesions and tumour samples. In part, our results contradict the ones of Hao et al. , which stated that both MCT1 and MCT4 are upregulated in prostate cancer tissue, however the percentage of MCT4 positivity for pT3 tumours (around 40%) is similar to ours (44% tumour positive cases). Since the number of cases analysed by these authors is only slightly smaller than ours, the differences observed may be due to the different antibodies used. The specificity of our antibodies was tested by western-blot and more recently by RNAi for MCT1 (data not shown). We also observed frequent and clear MCT1 membrane expression, while these authors state that MCT1 staining was mostly cytoplasmic. The granular appearance of MCT2 and MCT4 expression in the cytoplasm of prostate tumour cells, as well as the predominance of the strong immunostaining scores suggests that these MCT isoforms could have important functions in some organelle membranes, possibly playing a role in the metabolism of prostate tumour cells.
Importantly, MCT2 was the only marker which allowed distinction between adjacent non-neoplastic tissue and PIN lesions. For MCT1, MCT4 and CD147, expression was similar in both. Despite apparently normal to the Pathologist, adjacent non-neoplastic glands already present alterations from normal tissue.
Monocarboxylate transporters 1 and 4 expression is associated with CD147 in prostate cancer
A close association between CD147 expression and both MCT1 and 4 was found, similar to the findings of Hao et al. . Additionally, we detected no association with MCT2, supporting CD147 as chaperone for both MCT1 and MCT4 but not with MCT2 in prostate cancer. Studies of CD147 in paraffin-embedded specimens of prostate cancer are not many, however they describe overexpression of CD147 in prostate cancer, reporting expressions between 60 to 80% [22–25]. In the present study, we found around 50% of prostate tumour cases expressing CD147 and this expression was significantly different from the normal prostate tissue. To the best of our knowledge, our study has the biggest sample size and the number of non-neoplastic samples analysed is similar to the tumour samples.
Gp70 was only expressed in very few cancer cases and there was no association with either MCT isoforms. This result was surprising, however, since MCT2 was not present in the plasma membrane, the mechanism of regulation might be different. In addition, as described for CD147 and MCT isoforms 1 and 4 , there might be other chaperones involved in MCT2 regulation.
MCT4 and CD147 overexpression is associated with poor prognosis in prostate cancer
Assessment of associations between MCTs and CD147 expression and clinico-pathological data, revealed some important associations. In accordance to the work of other groups, we found positive associations between both MCT4 and CD147 expressions and higher PSA levels, advanced tumour stage and higher Gleason score [14, 22–25]. However, regarding tumour stage, the difference in MCT4 expression in the report of Hao and collaborators , appears to be only from pT1 to pT2 and 3 since the levels of the last two appear to be similar. In our series we do not have pT1 stage cases, which makes the comparison more difficult. Additionally, we found associations between MCT1 expression and higher PSA levels, absence of perineural invasion and presence of biochemical recurrence, as well as between both MCT4 and CD147 and presence of perineural invasion and biochemical recurrence, which to the best of our knowledge, was not described by others. MCT2 also correlated with lower age at diagnosis, while both MCT4 and CD147 were associated with higher age at diagnosis, which significance is not known.
The differences observed between our study and others, besides the use of different antibodies, might be also due to the diverse immunohistochemical assessment, while in the present study we considered both intensity and percentage of immunoreactive cells, other authors considered only either intensity or extension of staining [14, 22–25]. We believe that evaluating two parameters instead of one, decreases subjectivity and will have higher biological significance. Moreover, our non-neoplastic tissue was selected from the peripheral zone of the prostate in which prostate cancer is diagnosed and this may also have contributed to the differences observed.
Overall, we found no important clinicopathological associations with MCT2 but tumours that are highly positive (HSG) for MCT1, MCT4 or CD147, seem to exhibit a more aggressive behaviour, especially MCT4 and CD147 which correlated with higher PSA levels, higher pT stage, higher Gleason score, presence of perineural invasion and biochemical recurrence. However, to elucidate the significance of these associations, functional studies will be needed.
MCTs and prostate cancer metabolism
At variance with other solid tumours [6, 7, 9], we did not find up-regulation of MCT1, MCT4 or CD147 in the plasma membrane of prostate cancer cells, proteins normally involved in the hyper glycolytic-acid resistant phenotype of cancer cells. On the other hand, there was upregulation of MCT2 and MCT4 in the cytoplasm of cancer cells, with a granular appearance. These findings suggest two hypothesis: either presence of alternative mechanisms that ensure acid efflux and maintenance of intracellular pH, or presence of an alternative metabolic pathway different from glycolysis that predominates in prostate cancer. Indeed, β-oxidation pathway is suggested to be up-regulated in prostate cancer  and α-methylacyl-CoA racemase (AMACR), an enzyme involved in branched chain fatty acid β-oxidation, is already being explored as a diagnostic marker of prostate cancer . Additionally, MCT2, analysed for the first time in the present work, is involved in short-chain fatty acid transport and appears overexpressed and with strong staining in the cytoplasm of prostate tumour cells, with a granular appearance. These facts point to this MCT isoform as an important protein in prostate tumour cells, likely involved in some organelle function. In fact, the work of McClelland and collaborators provide evidence for a putative role of MCT2 in hepatocyte peroxisomal membrane .
In the present study, we analysed the expression of MCT1, MCT2, MCT4, CD147 and gp70, in prostate cancer, corresponding adjacent non-neoplastic tissue, normal tissue and PIN lesions, and sought for associations with the clinico-pathological data of the patients. Our data provides novel evidence for the involvement of MCTs in prostate tumours. According to our results, we believe that MCT2 should be further explored as tumour marker and MCT4 and CD147 as markers of poor prognosis in prostate cancer.
Acknowledgements and Funding
NPG, CP and VMG received fellowships from the Portuguese Foundation for Science and Technology (FCT), refs. SFRH/BD/61027/2009, SFRH/BPD/69479/2010 and SFRH/BI/33503/2008, respectively. This work was supported by the FCT grant ref. PTDC/SAU-FCF/104347/2008, under the scope of "Programa Operacional Temático Factores de Competitividade" (COMPETE) of "Quadro Comunitário de Apoio III" and co-financed by Fundo Comunitário Europeu FEDER.
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