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1 Nuffield Department Clinical Laboratory Sciences, John Radcliffe Hospital and 2 Department of Cardiovascular Medicine, Wellcome Trust Centre for Human Genetics, Henry Wellcome Building of Genomic Medicine, University of Oxford; and 3 Cancer Research UK Molecular Oncology Laboratory, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, United Kingdom
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ABSTRACT |
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and the CH1 domain of the transcriptional coactivator p300/CBP is necessary for the expression of hypoxia responsive genes and tumor angiogenesis. The transcription factor CITED2 binds p300/CBP at the CH1 domain and functions as a negative regulator of hypoxia signaling by competing with hypoxia-inducible factor 1. CITED4, a recently identified member of the CITED family, binds p300/CBP via the CH1 domain and functions as a coactivator for transcription factor AP-2. Here, we show that CITED4 blocks the binding of hypoxia-inducible factor 1 to p300 in vitro and inhibits hypoxia-inducible factor-1 transactivation and hypoxia-mediated reporter gene activation. These studies suggest that CITED4 might function as an inhibitor of hypoxia-inducible factor 1. To explore the function of CITED4 in breast cancer, we determined its expression in normal, in situ and invasive breast cancers. We also correlated its expression in 286 invasive breast tumors with clinicopathological, hypoxia markers and survival. In contrast to the nuclear localization of CITED4 in normal breast tissue, breast tumors were characterized by cytoplasmic and nuclear localization. Nuclear CITED4 expression was significantly inversely associated with tumor hypoxia-inducible factor 1 (P < 0.05), tumor size (P = 0.03), tumor grade (P = 0.0001), and Chalkley vessel count (P = 0.04). CITED4 showed no significant correlation with patient age (P = 0.45), estrogen receptor (P = 0.11), or epidermal growth factor receptor (P = 0.48). These results show that breast cancer development is characterized by either nuclear loss or cytoplasmic translocation of CITED4, with consequent loss of hypoxia-inducible factor-1 transcriptional antagonist activity. This may be an important mechanism by which tumors enhance hypoxia-inducible factor expression and result in an aggressive phenotype. |
INTRODUCTION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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is often a crucial step for the expression of angiogenic factors controlling tumor neovascularization. To activate transcription, hypoxia-inducible factor 1 must recruit the transcriptional adapter/histone acetyltransferase proteins, p300 and CBP to the target gene promoters. This occurs by direct physical interactions between the transactivation domain of hypoxia-inducible factor 1 and the first cysteine-histidine (CH1) domain of p300/CBP. This domain of p300/CBP also binds members of the CITED (CBP/p300 interacting transactivator with ED-rich tail) family of transcription factors via their conserved COOH-terminal transactivation domain. We have showed previously that CITED2 (also known as p35srj or Mrg1), a hypoxia- and growth factor-induced transcription factor, will disrupt the interaction between hypoxia-inducible factor 1 and p300 and inhibit transactivation by hypoxia-inducible factor 1 and gene activation by hypoxia (1
, 2)
. The solution structure of the hypoxia-inducible factor 1-p300 and the CITED2-p300 complexes provides a molecular mechanism for this competition. CITED2 binds with 33-fold greater affinity to CH1 in comparison to hypoxia-inducible factor 1. Both CITED2 and hypoxia-inducible factor 1 share a LPXL (Leu-Pro-X-Leu) motif that interacts with an overlapping binding site on p300-CH1 (3
, 4)
. Genetic evidence indicates that loss of CITED2 is associated with increased activation of hypoxia-inducible factor-1 target genes, supporting this model (5)
. CITED2 also functions as a coactivator for the transcription factor AP-2, linking it to p300/CBP (6
, 7)
. These interactions are thought to underlie the neural and cardiac developmental malformations associated with loss of CITED2 (5
, 6
, 8)
. CITED2 also functions to control cell proliferation and loss of CITED2 results in premature senescence of mouse embryonic fibroblasts. This results from a deficiency of Bmi1 and Mel18, which function to repress the cell proliferation inhibitors INK4a/ARF (9)
. We have identified recently a new member of the CITED family, called CITED4, and showed that it directly binds the p300-CH1 domain and functions as a coactivator for transcription factor AP-2 (10) . CITED4 is expressed ubiquitously in both human and mouse tissues. Cited4 expression is weak in nulliparous mouse breast tissues but is activated strongly by mid-gestation, with the protein showing a nucleocytoplasmic distribution. This high level of expression continues on through gestation and weaning. Consistent with this, Cited4 expression was stimulated by prolactin-induced differentiation of mouse mammary epithelial Scp2 cells in culture (11) .
The CITED4 transactivation domain is highly conserved with that of CITED2 and also contains the LPXL motif. This suggests that CITED4, like CITED2, may function as an inhibitor of hypoxia-inducible factor 1 transactivation. In this report, we test this hypothesis and show that CITED4 is able to inhibit hypoxia-inducible factor 1 by disrupting the interaction with p300. Because we have demonstrated previously expression of CITED4 in human breast cancer cell lines (10)
, and we have shown hypoxia to be an important microenvironmental influence in breast cancer (12)
, we also examined the expression of CITED4 and hypoxia-inducible factor 1 in breast carcinomas. Our findings show that tumors are able to down-regulate expression of CITED4 or translocate CITED4 to the cytoplasm, which is associated with elevated hypoxia-inducible factor 1 and increased tumor size, grade, and angiogenesis.
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MATERIALS AND METHODS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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chains.
CITED4 Regulation of Hypoxia-Inducible Factor 1
Plasmids.
Plasmids expressing CITED4 full-length or truncated CITED4 lacking the p300/CBP interacting domain (CITED4
), untagged or HA-tagged, have been described previously (10)
. GAL4-hypoxia-inducible factor 1 and hypoxia-inducible factor 1 expressing plasmids used for generating 35S-labeled peptides have been described previously (1
, 14)
. The GAL4-luc reporter and pCMV-lacZ plasmids were gifts from Ron Evans (Salk Institute, San Diego, CA). The 3xHRE-TK-luc reporter (15)
was a gift from Steve McKnight (University of Texas, Dallas, TX).
GST Fusion-Binding and Peptide Competition.
GST fusion proteins were generated as described previously (16)
. 35S-labeled peptides were synthesized using a TNT kit (Promega) following the manufacturer’s instructions. In vitro binding reactions were done as described previously (1)
. Peptides used for competition experiments were DEEALTSLELELGLHRVRELPELFLGQSEFDCF (residues 138–170 of human CITED4) and YAGPGMDSGLRPRGA (residues 32–46 of mouse CITED4). GST-p300-CH1 or GST (1 µg of eluted protein) was preincubated with the indicated peptide (20 µg) for 5 hours in 300 µl Hyb-75 + 1% milk buffer. All of the reaction mixtures contained equal amounts of the DMSO vehicle used to dissolve the peptides. 35S-labeled, in vitro translated proteins were then added, and binding reactions were carried out overnight, after which the relevant proteins were precipitated with glutathione-Sepharose beads and analyzed as described above.
Tumors and Patients
Breast carcinomas (n = 286) and normal tissue from reduction mammoplasties (n = 6) were collected from patients undergoing surgery at the Oxford Radcliffe Hospitals (Oxford, United Kingdom). Tumors were treated by simple mastectomy (n = 71) or lumpectomy (n = 215) with axillary node sampling. All of the patients with tumors had axillary node status confirmed histologically. Histological types included 205 ductal carcinomas not otherwise specified, 20 lobular carcinomas, and 21 other types (data unavailable for 40 tumors). Grading of carcinomas was done according to the modified Bloom and Richardson method. The clinicopathological characteristics are given in Table 1
. In patients <50 years, adjuvant cyclophosphamide, methotrexate, and 5-fluorouracil i.v. for six courses was administered if tumors were node-positive or estrogen receptor-negative and/or 
3 cm. Patients 50 years with estrogen receptor-negative, node-positive tumors also received cyclophosphamide, methotrexate, and 5-fluorouracil. Patients with estrogen receptor-positive tumors received tamoxifen for 5 years; median follow-up was 7.3 years (range 0.4–11.0) and patients showed 97 relapses and 74 deaths.
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Four-micron sections from formalin-fixed paraffin-embedded tissues from both series were cut onto silane-coated slides. These were dewaxed through xylene and graded alcohols, before placing in PBS for 5 minutes. Primary antibody (HT13; for characterization see Results) was applied as neat supernatant for 30 minutes without any antigen-retrieval techniques, followed by EnVision (Dako, United Kingdom) detection system.
In a preliminary analysis, some tumors were noted to be negative for CITED4, whereas others showed immunopositivity in the nucleus and/or cytoplasm of neoplastic cells. Because p300 and CBP are nuclear proteins and hypoxia-inducible factor-p300 interactions occur in the nucleus, it is likely that CITED4 physical inhibition of hypoxia-inducible factor 1 at the CH1 domain also takes place in the nucleus. Therefore, we stratified tumors into functionally negative for CITED4 (i.e., no or <10% nuclear staining) and functionally positive for CITED4 (tumors that showed 10% nuclear staining).
Assessment of Hypoxia-Inducible Factor 1 Expression, Vascular Endothelial Growth Factor (VEGF), and Microvessel Quantitation
The hypoxia-inducible factor 1 protein was detected using the monoclonal antibodies ESEE 122 (IgG1; dilution 1:40; ref. 12
) and the Envision-HRP kit (DAKO, Glostrup, Denmark). The intensity of nuclear staining was compared with that seen in parallel stained-control sections, as reported previously, with scoring based on the intensity and extent of nuclear and cytoplasmic reactivity (12)
. Cases with absent or weak cytoplasmic expression of hypoxia-inducible factor were considered as negative. Cases with nuclear expression or strong cytoplasmic expression were considered as positive.
To assess whether localization of CITED4 was related to function of hypoxia-inducible factor 1, this transcription factor together with the hypoxia-inducible factor-1 target gene VEGF was analyzed. VEGF expression was semiquantitatively scored on the cytoplasmic tumor intensity and proportion of cell expressing VEGF, using VG1 (17
, 18)
. Chalkley vascular counts were quantitatively determined by assessing the three most vascular areas at x250 magnification, as reported previously (19)
. Two observers assessed the stainings using a conference microscope.
Statistical Analysis
Spearman rank correlation coefficients were used for studying the association between continuous variables. Tests of hypotheses on the location parameter (median) were done using rank statistics (Mann-Whitney, Kruskall-Wallis, and adjusted Kruskall-Wallis for ordered groups). The chi-square test was used to test for independence of categorical variables including categorized continuous variables. The log-rank test was used to test for differences in survival, and Cox proportional hazards model was used for multivariate models of survival. All of the statistics were done using the Stata package release 7.0 (Stata Corporation, College Station, Texas).
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RESULTS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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), were transfected with a plasmid expressing NH2-terminal HA-tagged CITED1, CITED2, and CITED4 human genes. The whole cell extracts prepared from the transfected U2-OS cells were separated on SDS-PAGE and immunoblotted with the anti-HA antibody or HT13 (Fig. 1 A
, top and middle panels, respectively). The anti-HA antibody detected HA-tagged CITED1, CITED2, and CITED4 peptides (Fig. 1A
, top panel), indicating that the three CITED peptides were expressed in the transfected cells. When HT13 was used, only HA-CITED4 peptide was detected, indicating that HT13 does not cross-react with the other closely related CITED peptides and is highly specific for CITED4 peptide.
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. A specific band with a molecular weight (Mr 
24,500) similar to the human CITED4 was detected in ECV304 but not in MDA-MB-231 protein extracts. This again indicates that HT13 detects CITED4 specifically.
We then examined the specificity of HT13 for CITED4 detection by immunostaining. U2-OS cells were transfected with plasmids expressing NH2-terminal HA-tagged CITED1, CITED2, or CITED4 peptides. The cells were immunostained simultaneously with HT13 and with a rat anti-HA-tag antibody (Fig. 1C)
. The HA-antibody was able to detect all of the HA-CITED proteins (Fig. 1C
, panels b–d, green), whereas HT13 specifically detected HA-CITED4 peptide (Fig. 1C
, panel b, red). Both signals detected in cells transfected with the plasmid-expressing HA-CITED4 colocalized, indicating that the HA-CITED4 peptide was detected simultaneously by the anti-HA and HT13 antibodies. The HA-tagged CITED4 peptide was detected mainly (by both antibodies) in the cytoplasm of transfected U2-OS cells. But in some cells, HA-CITED4 also localizes in the nucleus (Fig. 1C
, panel b).
The Effect of CITED4 on Hypoxia-Activated Transcription.
We used GAL4-hypoxia-inducible factor 1, a fusion of hypoxia-inducible factor 1 residues 723–826 to the GAL4 DNA-binding domain to test whether CITED4 affects hypoxia-inducible factor 1 transactivation. These hypoxia-inducible factor 1 residues bind p300-CH1 and constitute a transactivation domain. Cotransfection of GAL4-hypoxia-inducible factor 1 with a GAL4-luciferase reporter plasmid into cells activated the luciferase gene only after stimulation by hypoxia (Fig. 2A)
. Cotransfection of a CITED4-expression plasmid (HA-CITED4) led to a complete loss of induced GAL4-hypoxia-inducible factor 1 transcriptional activity. A CITED4 mutant lacking the p300-CH1 binding domain (HA-CITED4) failed to interfere with GAL4-hypoxia-inducible factor 1 transcriptional activity. In analogous experiments, CITED4 also inhibited the transactivation function of GAL4-EPAS1/hypoxia-inducible factor 2 (residues 19–870; data not shown).
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. A reporter plasmid containing the luciferase gene under the control of three hypoxia-inducible factor 1 consensus DNA-binding elements (3xHRE-luc) was used to assess the effect of CITED4 expression on endogenous hypoxia-inducible factor 1 activity. As shown in Fig. 2B
, transcription from the transfected reporter gene is activated when cells are stimulated by hypoxia, and this is markedly inhibited by CITED4. The inhibition conferred by CITED4 is dependent on the presence of its COOH-terminal domain, because the expression of CITED4 is unable to suppress hypoxia-stimulated transcription.
The Effect of CITED4 on Hypoxia-Inducible Factor 1 Interaction with p300-CH1.
To determine the biochemical mechanism by which CITED4 inhibited transactivation by hypoxia-inducible factor 1, we generated 35S-labeled hypoxia-inducible factor 1 by coupled in vitro transcription-translation. This peptide was tested for interaction with bacterially expressed purified GST-p300-CH1 fusion protein (containing GST fused to p300 residues 300–528; Fig. 2C
, Lane 3). This experiment showed that, in vitro, hypoxia-inducible factor 1 interacts with the CH1-domain of p300. To determine whether CITED4 would affect its binding, we performed a similar in vitro binding experiment in the presence of a peptide corresponding to residues 138–170 of CITED4, which is homologous to the p300-CH1 binding domain mapped previously in CITED2 (1)
. Addition of the CITED4 peptide in the reaction mix led to a hypoxia-inducible factor 1 decreased binding to the p300-CH1 domain (Fig. 2C
, Lane 4). A control peptide derived from the NH2 terminus of CITED4 had no effect (Fig. 2C
, Lane 5).
The Pattern of Expression of CITED4 in Normal and Neoplastic Breast Tissues.
Whole tissue sections of all of the normal and in situ carcinomas together with 86 invasive tumors were stained satisfactorily. Expression of CITED4 was observed in normal breast tissues. This was present in epithelial elements, mostly in the ductal cell but also in myoepithelial cell layers (Fig. 3A and B)
. Occasional cases showed strong myoepithelial cell without ductal cell staining. Expression was also identified in other elements, including inter- and intralobular stroma and occasional endothelial cells. Expression was mostly nuclear but also cytoplasmic (Fig. 3C)
.
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. Expression was observed in both in situ and invasive disease (Fig. 3, D–G)
. Expression was present mostly in the cytoplasm of malignant epithelium. In in situ disease, staining was heterogeneous and weak (Fig. 3E)
, whereas in invasive carcinomas, it was homogenous and generally stronger (Fig. 3, F–G)
. In 30 cases, tumor-associated microvessels were also positive for CITED4. Stromal staining was frequently present, and occasional cases were also positive in arteriolar smooth muscle and pericytes (Fig. 3G
, inset). In tissue microarrays, 124 cases showed no or <10% nuclear staining and 162 10% nuclear staining. Forty-nine cases showed no cytoplasmic expression, 106 weak, 91 moderate, and 40 strong cytoplasmic staining.
Relationship among Tumor CITED4 Protein Expression and Clinicopathological, Microvessel Density, Hypoxic Markers, and Survival.
To investigate additionally the change in location from nuclear to cytoplasmic compartment, we examined the relationship among potentially functional (conserving nuclear expression) and nonfunctional (no nuclear expression) CITED4 and clinicopathological variables and survival. This stratification split the tumors such that 124 were considered to lose CITED4 function and 162 were considered to have retained it. We observed significant inverse associations between retention of nuclear CITED4 and tumor hypoxia-inducible factor 1 expression (P < 0.05), tumor size (P = 0.03), tumor grade (P = 0.0001), and Chalkley vessel count (P = 0.04; Table 1
). CITED4 showed no significant correlation with patient age (P = 0.45), estrogen receptor (P = 0.11), or epidermal growth factor receptor (P = 0.48; Table 1
). In a survival analysis, patients with CITED4 function positive tumors had an improved relapse-free and overall survival of borderline significance (P = 0.06; Fig. 4
).
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DISCUSSION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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antagonist through a functionally critical sequence motif (LPXL), and we tested whether CITED4, which also contains the identical motif, could act in a similar manner. Our results show that cotransfection of CITED4 efficiently inhibited hypoxia-inducible factor 1 transcriptional activity, and that this effect requires the p300-CH1 binding domain of CITED4. We show additionally that CITED4 strongly inhibits the interaction of p300-CH1 with hypoxia-inducible factor 1 in vitro, indicating that the transcriptional inhibitory effects of CITED4 are because of direct competition for available p300/CBP binding sites.
Because CITED4 is expressed in murine mammary tissues, in human breast cancer cell lines, and hypoxia is an important microenvironmental influence in breast cancer biology (10, 11, 12)
, we also examined the expression of CITED4, hypoxia-inducible factor 1, and the hypoxia-inducible factor 1 target gene VEGF in breast cancer. In normal breast tissues, CITED4 was expressed in several tissue elements with a predominant nuclear distribution, consistent with a role in the normal physiological changes in the breast that occur during the menstrual cycle. In support of this is differential expression of different CITED proteins during the murine milk cycle and changes in their expression between nulliparous and pregnant breast tissues (10
, 11)
. Nevertheless, unlike breast tissues in the mouse, we identified expression of CITED4 in nonepithelial tissue elements, suggesting the role of CITED4 in human tissues is more complex.
In contrast to normal breast tissue, CITED4 in tumors showed several patterns of cellular location. These included retention of nuclear expression, cytoplasmic expression, and no expression. Using a rabbit polyclonal antibody, we have shown previously that CITED4 is predominantly in the nucleus in ECV304 cells (10)
. However, CITED1 expression is exclusively cytoplasmic in keeping with the ability of these proteins to be expressed in different cellular compartments (20)
. Thus, it is possible that during neoplastic transformation, tumors either suppress CITED4 and/or locate it in the cytoplasmic compartment, physically distancing CITED4 from binding p300/CBP and, thus, allowing enhanced hypoxia-inducible factor 1 function with increased effectiveness of any given level of hypoxia-inducible factor 1. A change in nuclear cytoplasmic location of many proteins has been noted in breast cancer and other tumor types and may represent a change in regulation of these proteins (21)
. In additional support of this notion is the observation of a less aggressive tumor phenotype in tumors retaining nuclear expression with improved survival in the univariate analysis. Nevertheless, this was not independent in a multivariate analysis, which is likely to be because of the strong associations with tumor grade, size, and Chalkley vessel count.
There is increasing evidence of multiple pathways that may synergize with hypoxia to regulate hypoxia-inducible factor 1 in cancer, including PTEN mutation, Ras activation, and growth factor signaling pathways (22)
. We describe a novel pathway, the cytoplasmic localization of a transcriptional antagonist by which hypoxia-inducible factor may also be regulated. The intracellular processing of CITED4 in tumor cells may occur through several mechanisms, including increased cytoplasmic binding or decreased nuclear import/export. Although we have been unable to show additional nuclear CITED4 accumulation in Hep3b or T47D cells (which mainly localizes in the cytoplasm) with leptomycin B (data not shown), suggesting cytoplasmic binding as the likely mechanism, reports of nuclear export insensitive to leptomycin B have been described previously (23)
. The cytoplasmic export has been reported for several other nuclear proteins including p53, mdm2, and p21 (24
, 25)
that would also similarly affect function. In keeping with this, CITED1 is reported to show exclusive nuclear expression in human melanoma (20)
.
It is unlikely that CITED4 is directly regulating hypoxia-inducible factor 1 expression, but clearly the pathways converge and are selected in tumor biology. Although not addressed in this study, it is possible that displacement of hypoxia-inducible factor 1 from p300/CBP allows it to be more efficiently targeted for degradation by the von Hippel-Lindau-ubiquitin ligase complex. Additionally, the association of high nuclear hypoxia-inducible factor 1 and the cytoplasmic antagonist CITED4 would be associated with more aggressive phenotypes, as reported here for CITED4 and by others for hypoxia-inducible factor 1 (26)
.
In addition to being a transcriptional inhibitor, CITED4 is a strong coactivator for AP2, which is able to up-regulate VEGF (27) . However, in agreement with other studies (28) , we observed no relationship between tumor cell CITED4 function and VEGF expression, which may be because of cell-type specific AP2 coactivation, or, more likely, that human tumors use several pathways to regulate VEGF, such as Sp-1, AP-1, CREB-1, and RTEF-1. Nevertheless, the exact role of AP2 in breast cancer is also unclear, because AP2 overexpression is associated with high expression of HER2 and estrogen receptor in breast cancer cell lines (29) but low AP2 levels with disease progression (30) . In the latter study, AP2 localized to the cytoplasm in half of the carcinomas (30) , again indicating the aberrant localization of transcriptional regulators in cancer.
In summary, we have shown that CITED4 strongly inhibits the interaction of p300-CH1 with hypoxia-inducible factor 1 and is an efficient inhibitor of transactivation by hypoxia-inducible factor 1. We have observed that in tumors, there is an alteration in the expression pattern of CITED4 from nucleus to cytoplasmic. This loss may allow p300/CBP to interact with hypoxia-inducible factor 1 and oncogenes to enhance their transcriptional activity leading to an aggressive tumor phenotype. Because CBP/p300 has been reported to function as a transcriptional coactivator of BRCA1 (31)
, it would be of interest to assess the expression of CITED4 in breast cancers derived from BRCA1-affected individuals. Study into enhancing the effect of CITED4 to interfere with hypoxia-inducible factor function is warranted, particularly because it does not have a nuclear localization signal. It may be possible to generate small molecules that bind particular elements CITED4-hypoxia-inducible factor-1-p300 complex and differentially affect components of the hypoxia response (4)
.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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Requests for reprints: Stephen B. Fox, Nuffield Department Clinical Laboratory Sciences, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DU, United Kingdom. Phone: 44-1865-222783; Fax: 44-1865-228980; E-mail: stephen.fox{at}ndcls.ox.ac.uk
Received 2/26/04. Revised 4/30/04. Accepted 6/30/04.
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REFERENCES |
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and carbonic anhydrase IX in human tumours. J Clin Pathol, 57: 504-12, 2004.This article has been cited by other articles:
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  G. Shi, S. C. Boyle, D. B. Sparrow, S. L. Dunwoodie, T. Shioda, and M. P. de Caestecker The Transcriptional Activity of CITED1 Is Regulated by Phosphorylation in a Cell Cycle-dependent Manner J. Biol. Chem., September 15, 2006; 281(37): 27426 - 27435. [Abstract] [Full Text] [PDF]
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 A. Bottini, D. Generali, M. P. Brizzi, S. B. Fox, A. Bersiga, S. Bonardi, G. Allevi, S. Aguggini, G. Bodini, M. Milani, et al. Randomized Phase II Trial of Letrozole and Letrozole Plus Low-Dose Metronomic Oral Cyclophosphamide As Primary Systemic Treatment in Elderly Breast Cancer Patients J. Clin. Oncol., August 1, 2006; 24(22): 3623 - 3628. [Abstract] [Full Text] [PDF]
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 L. L. Nikitenko, N. Blucher, S. B. Fox, R. Bicknell, D. M. Smith, and M. C. P. Rees Adrenomedullin and CGRP interact with endogenous calcitonin-receptor-like receptor in endothelial cells and induce its desensitisation by different mechanisms. J. Cell Sci., March 1, 2006; 119(Pt 5): 910 - 922. [Abstract] [Full Text] [PDF]
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 S. Plisov, M. Tsang, G. Shi, S. Boyle, K. Yoshino, S. L. Dunwoodie, I. B. Dawid, T. Shioda, A. O. Perantoni, and M. P. de Caestecker Cited1 Is a Bifunctional Transcriptional Cofactor That Regulates Early Nephronic Patterning J. Am. Soc. Nephrol., June 1, 2005; 16(6): 1632 - 1644. [Abstract] [Full Text] [PDF]
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