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A major challenge is to identify the physiological relevance of cancer-associated genetic polymorphisms. Several changes in the coding sequence of β integrin subunits have now been described in human tumours. One of these, T188Iβ1, was identified as a heterozygous mutation in a poorly differentiated squamous cell carcinoma (SCC) and shown to activate extracellular matrix adhesion and inhibit keratinocyte differentiation in vitro. To study its contribution to tumour development, we overexpressed the mutant or wild-type (WT) human β1 subunit in the basal layer of mouse epidermis using the keratin 14 promoter. The transgenic integrins were expressed at the cell surface and were functional, T188Iβ1 promoting cell spreading to a greater extent than WTβ1. Epidermal proliferation and differentiation were unaffected and no expansion of the stem cell compartment was detected. During chemical carcinogenesis both transgenes increased papilloma formation, but only the T188Iβ1 transgene stimulated conversion of papillomas to SCCs. Papillomas bearing the mutation showed increased Erk activity and reduced differentiation. SCCs expressing T188Iβ1 were less well differentiated than those expressing WTβ1. These observations establish that expression of a genetic variant in the I-like domain of β1 integrins does not affect normal epidermal homeostasis, but increases tumour susceptibility and influences tumour type.
Integrin extracellular matrix receptors regulate many aspects of epidermal cell behaviour (1). Within the basal layer of human epidermis stem cells express higher levels of integrins than cells that are committed to undergo terminal differentiation (2-4). Integrin signalling to Erk/MAPK plays a role in maintenance of the stem cell compartment (5, 6). Studies with cultured human epidermal cells show that integrin ligation suppresses the onset of terminal differentiation, with ligated integrins sending a ‘do not differentiate’ signal to the cells (7, 8). In mouse models, epidermal-specific deletion of specific integrins leads to a range of phenotypes, from epidermal blistering to a failure to maintain the hair follicles (1, 9, 10).
Integrins are implicated in a variety of epidermal diseases (1, 11-16). Integrin expression or signalling is often altered in squamous cell carcinomas. In studies of chemically induced skin carcinogenesis, overexpression of integrins in the suprabasal layers alters susceptibility to tumour development (17-19).
We previously identified a heterozygous mutation in the β1 integrin subunit in cells from a poorly differentiated human SCC of the tongue (20). The mutation, T188I, lies in the specificity loop of the I-like domain (21, 22) and results in constitutive activation of ligand binding, thereby stimulating cell spreading at low extracellular matrix concentrations (20). While expression of the mutation in cultured cells does not affect cell migration or invasion, it does lead to enhanced activation of Erk/MAPK signalling (20). In contrast to the wild-type β1 subunit, unligated T188Iβ1 does not trigger initiation of terminal differentiation in human keratinocytes (20).
Sequencing of the β1 I-like domain in 124 human head and neck squamous cell carcinomas has revealed several additional single nucleotide changes, one of which results in a change in amino acid sequence (A239V) (23). The same single nucleotide changes are present in normal tissue from the patients, indicating germline polymorphisms. In addition, sequencing by the Sanger Cancer Genome Project1 has identified two cancer-associated amino acid changes in the I-like domain of the β6 integrin subunit (P184S and N195Y). We conclude that changes in the amino acid sequence of β integrin I-like domains are found at low frequency in tumours and that they are probably polymorphisms rather than somatic mutations. In order to investigate the physiological role of the T188I mutation we expressed the human T188Iβ1 mutant or the wild-type human subunit in the epidermis of transgenic mice.
Human wild-type and T188I mutant β1 integrin subunit cDNAs (24) were subcloned into the BamHI restriction site of the keratin 14 (K14) promoter cassette kindly provided by E. Fuchs and injected into the male pronucleus of day 1 fertilized FVB/N mouse eggs. Potential founder lines were screened by PCR using one primer specific for β-globin (TACTCTGAGTCCAAACCGGGC) and one specific for the human integrin β1 subunit (CAATTTGGCCCTGCTTGTATACATTCTCCA). K14T188Iβ1 founder lines were 4826B, 4828B (low) and 4828B (high). K14WTβ1 founders were 4898A and 4837A. Founder lines 4828B (low) and 4837A had lower transgene copy numbers than the other lines.
Experiments were subject to CR-UK ethical review and performed under the terms of a UK Government Home Office licence. BrdU injections were performed as previously described (25).
Chemical carcinogenesis experiments were performed on seven week-old female K14WTβ1 (line 4898A), K14T188Iβ1 (4828B, high) mice and non-transgenic littermates (25 animals/group), essentially as described previously (17-19). Mice received one topical application of 100 nmol (25 μg) 7,12-dimethylbenz[a]anthracene (DMBA; Sigma-Aldrich; St Louis, MO) in 200 μl acetone followed by twice weekly applications of 6 nmol (3.7 μg) 12-O-tetradecanoylphorbol-13-acetate (TPA; Sigma-Aldrich; St Louis, MO) in 200 μl acetone. As controls, transgenic and non-transgenic littermates (5-10 animals/group) were subjected to the same protocol but substituting DMBA or TPA with acetone.
Papillomas and SCC were recorded once per week for up to 54 weeks after the start of promotion. Tumour sections were graded as described previously (17).
For sections, tissue was fixed in 10% neutral-buffered formalin and embedded in paraffin or frozen in liquid nitrogen-cooled isopentane and then embedded in OCT embedding matrix (Raymond A Lamb, UK). Epidermal whole mounts of tail skin were prepared as described previously (25), with minor modifications.
The following monoclonal antibodies were used: AIIB2, TS2/16, DH12 and P5D2 (anti-human β1 integrin subunit; Developmental Studies Hybridoma Bank, Iowa City, IA) (26, 27); LHK15 (anti-keratin 15; 25); anti-BrdU (Clone 3D4, BD Pharmingen; San Jose, CA); MB1.2 (anti-mouse β1 integrins; 25); and GoH3 (anti-integrin α6 chain; BD Pharmingen). Rabbit antibodies were: anti-phospho p44/42 MAPK (Thr202/Tyr204) and anti-p44/42 MAPK (Cell Signaling Technology, Inc., Danvers, MA); anti-mouse keratin 14 (Covance Research Products, Inc; Denver, Pennsylvania); anti-laminin (Sigma-Aldrich; St Louis, MO); and anti-Ki67 (Neomarkers, Fremont, CA). AlexaFluor 488- or 594-conjugated secondary antibodies were obtained from Invitrogen Corp., Paisley, UK. Donkey anti-rabbit biotin antibody was from Jackson Laboratory; Bar Harbor, Maine.
Ki67, laminin and phosphorylated Erk were detected with the Bond Intense R Detection kit (Leica Microsystems; Wetzlar, Germany) in formalin-fixed paraffin-embedded sections following antigen-retrieval. Sections were photographed and analysed using the Ariol SL-50 system (Applied Imaging Corp., San Jose).
For immunofluorescence staining, frozen sections were fixed in 4% PFA/PBS for 10 minutes; paraffin sections were dewaxed and re-hydrated. Sections were permeabilized in 0.3% Triton X-100 for 5 minutes and blocked with 2% BSA, 0.02% fish skin gelatin and 10% fetal calf serum for 2 hours in PBS at room temperature. Sections were incubated in primary antibody overnight at 4°C, washed in PBS and incubated with secondary antibody for 45 minutes at room temperature.
Keratinocytes were isolated from 7-8 week-old mouse dorsal skin (28) and cultured on confluent J2-3T3 feeders in type I collagen coated flasks in calcium-free FAD medium supplemented with 10% FCS, hydrocortisone, insulin, cholera toxin and EGF. Spontaneously immortalised lines arose after approximately 10 passages.
The growth rates of immortalised lines were compared by plating 5 × 104 cells per well in 6 well plates in complete KSFM (Gibco) without feeders. Wells were pre-coated with 10 μg/ml human plasma fibronectin. Triplicate wells were harvested per time point. Cell number was determined using the CellTiter96Aqueous One Solution Cell Proliferation Assay kit from Promega, measuring absorbance at 490 nm.
To determine colony forming efficiency, 400 or 2000 primary keratinocytes were plated per well in 6-well type I collagen coated plates (BD Pharmingen). After 14 days, cultures were fixed and stained with 1% Rhodamine B and 1% Nile Blue (Acros Organic, Geel, Belgium) (2). Colony-forming efficiency was defined as percentage of plated cells that formed a colony of three or more cells.
Single cell suspensions were incubated for 20 min on ice with anti- β1 integrin antibodies diluted in pre-chilled PBS. After washing in chilled PBS cells were incubated with appropriate secondary antibodies as before. Flow cytometric analysis was performed using the FACS Calibur (BD FACSCalibur System, BD Biosystems) and Flow Jo software (Tree Star Inc.; Ashland, OR), excluding dead, 7AAD positive, cells and differentiated cells with high forward and side scatter.
96-well microtiter plates were coated with 50 μl human plasma fibronectin (Chemicon; Billerica, MA) or human placenta laminin (Sigma-Aldrich; St Louis, MO) overnight at 4°C and blocked with 1% heat-denatured BSA in PBS. 2 × 104 cells were added per well and incubated at 37°C for 30 min in serum-free medium containing 0.5% BSA. After washing, cells were fixed with 4% PFA in PBS and stained with Diff-Quik (International Reagents, Japan). Spread cells (defined as cells in which the long axis was more than twice the diameter of the nucleus) were counted in three independent fields/well. In some experiments cells were incubated with 10 μg/ml P5D2 antibody for 20 min at room temperature prior to plating.
To visualise F-actin, cells were fixed with 4% PFA in PBS for 10 min, permeabilised with 0.1% Triton X-100/PBS for 5 min and stained with phalloidin-conjugated Alexa-555 (Invitrogen Corp.; Paisley, UK).
Adherent subconfluent keratinocytes were surface-labeled with 1 mg/ml EZ-Link Sulfo-NHS-LC-Biotin (PIERCE; Rockford, IL)/PBS (-) (pH 8.0) for 15 min at room temperature. Cells were washed twice with serum-free, calcium-free FAD medium and incubated in complete medium at 37°C for 0, 4, 8 or 20h. Cells were harvested with trypsin/EDTA, incubated with P5D2 antibody for 30 min on ice and washed twice with ice-cold PBS. Pellets containing 4 × 106 cells were lysed in RIPA buffer (0.1% SDS, 0.5% sodium deoxycholate, 1% Nonidet P-40, 50 mM Tris-HCl (pH 8.0), 150 mM NaCl) with proteinase inhibitors (Roche; Basel, Switzerland). Cell lysates were clarified by centrifugation, then 20 μl of a 50% slurry of UltraLink Immobilized Protein G Plus Gel (PIERCE; Rockford, IL) was added and incubated for 1h at 4°C with gentle agitation. Beads and immune complexes were washed 3 times with 0.5% Nonidet P-40, 0.6M NaCl, 50 mM Tris-HCl (pH 8.3), resuspended in SDS-PAGE sample buffer without added reducing agent, boiled for 3 min, and resolved on 4-12% gradient polyacrylamide gels.
Following SDS-PAGE, separated proteins were transferred to PVDF membranes, blocked with 5% skim milk in TBS for 30 min and incubated with Extravidin-peroxidase (Sigma-Aldrich; St Louis, MO) in RIPA buffer for 1h at room temperature. After washing, Extravidin-peroxidase was visualized by ECL reagents (Amersham; Buckinghamshire, UK).
Cells were starved overnight in serum-free, calcium-free FAD. 3.5 × 105 cells were plated per 60 mm dish on 10 μg/ml fibronectin in the same medium supplemented with 0.5% BSA. Protein lysates were prepared in RIPA buffer containing protease and phosphatase inhibitors. Lysates were examined by Western blotting, essentially as described above, except that nitrocellulose membrane was used and the blocking buffer consisted of 2.5% skim milk powder and 0.05% Tween 20.
We used the keratin 14 (K14) promoter to target transgene expression to the known locations of epidermal stem cells (29). We initially compared three transgenic lines expressing the T188I mutant β1 subunit (T188Iβ1) and two expressing the human wild-type subunit (WTβ1). Mice from all founder lines were viable and fertile and none had any gross phenotypic abnormalities. We selected one founder line expressing each transgene for further analysis.
Transgene expression was confirmed by radioactive in situ hybridisation using a probe specific for the human β1 integrin. No signal was detected in sections of non-transgenic mice (NT; Figure 1A). In mice expressing either the wild-type human β1 subunit (K14WTβ1) or the mutant (K14T188Iβ1) the transgene was detected in the basal layer of the interfollicular epidermis, the sebaceous gland and hair follicle outer root sheath (Figure 1A). Using antibodies specific for the human (Figure 1B) or mouse (Figure 1C) β1 integrins we confirmed that the transgene-encoded integrins were co-expressed with the endogenous β1 integrins. However, in K14WTβ1 epidermis staining for endogenous β1 integrin was reduced (Figure 1C).
Cell surface β1 integrin levels were examined in primary keratinocyte cultures or immortalised keratinocyte lines. Cells were labelled with TS2/16 or DH12, two monoclonal antibodies to the human β1 integrin, or MB1.2, specific for mouse β1 integrins (Figure 1D). Flow cytometry established that cells from K14WTβ1 and K14T188Iβ1 transgenic mice expressed similar levels of human β1 integrins, with the caveat that the T188I mutation may affect the epitopes detected by the antibodies (Figure 1D). In cells expressing either transgene, the level of surface mouse β1 integrins was decreased relative to transgene-negative control cells, the effect being more marked in cells expressing the wild-type transgene (Figure 1C, D).
Downregulation of the endogenous mouse β1 integrin is expected, because surface levels of the β1 subunit are dependent on availability of endogenous α subunit partners (30). However, the fact that mouse β1 was not completely lost from the cell surface indicates that the T188Iβ1 mutant integrin was co-expressed on the cell surface with wild type (mouse) β1 (20).
To compare the turnover time of the transgene-encoded human β1 integrins (31), adherent keratinocytes were surface-labelled with biotin, chased for different periods of time and immunoprecipitated with P5D2 (Figure 2A). Consistent with the flow cytometry data, the levels of expression of WTβ1 and T188Iβ1 were similar. Two bands were detected by immunoprecipitation, corresponding to the mature β1 subunit and its α partners. Between 0 and 8 hours, the levels of the WT and mutant human β1 subunits were unchanged. By 20 hours, surface levels of both mutant and wild-type subunits had decreased to a similar extent. P5D2 displayed weak cross-reactivity with the endogenous mouse β1 integrin, and immunoprecipitation of surface labelled transgene-negative keratinocytes revealed that the kinetics of loss from the cell surface were similar to those of the transgene-encoded integrins (Figure 2A).
To examine Erk MAPK activation in transgenic keratinocytes, starved cells were plated on fibronectin for up to 150min (Figure 2B). The kinetics of Erk MAPK activation were similar in nontransgenic and K14WTβ1 transgenic cells. However, in K14T188Iβ1 transgenic cells Erk MAPK activation was greater at all time points examined (20). The ratio of phosphoErk to total Erk band intensity at 40 min was 0.34 for nontransgenic cells, 0.27 for K14WTβ1 cells and 1.63 for K14T188Iβ1 cells. In spite of the increased Erk activation, the T188I mutation did not increase the growth rate of immortalised keratinocytes on fibronectin-coated dishes under feeder-free, low calcium culture conditions (Figure 2C).
We next examined adhesion on fibronectin, which is mediated by α5β1, and laminin-10, which is mediated by α3β1 and α6β4 in combination (1). On fibronectin, transgene-positive keratinocytes adhered and spread to a greater extent than transgene-negative keratinocytes. The effect was greatest in cells expressing T188Iβ1 plated on low fibronectin concentrations (20) (Figure 2D). T188Iβ1 was also more effective than WTβ1 in promoting polymerisation of the actin cytoskeleton in cells plated on fibronectin, as evidenced by more intense labelling with phalloidin (Figure 2A). Adhesion of transgenic keratinocytes was markedly reduced by incubation with the anti-human β1 antibody P5D2. In contrast, P5D2 had no effect on transgene-negative keratinocytes (Figure 2D).
Keratinocyte adhesion and spreading on laminin-10 were similar in transgene-negative and positive keratinocytes, as predicted because of the role of α6β4 (1) (Figure 2D). Nevertheless, the transgene-encoded β1 integrins did contribute, since adhesion of transgenic keratinocytes to laminin-10 could be partially inhibited by P5D2 (Figure 2D).
Comparison of the histology of adult back skin from transgenic mice and transgene-negative littermate controls did not reveal any differences in the interfollicular epidermis (IFE), hair follicles (HF) or sebaceous glands (SG), and there was no evidence of a dermal inflammatory infiltrate (Figure 3A). Proliferation was evaluated by staining sections of adult back skin for Ki67 (data not shown) and by measuring BrdU incorporation into S phase cells in tail epidermal whole mounts (Figure 3B). K14WTβ1 and K14T188Iβ1 transgenic mice exhibited a similar number of proliferative cells in the back and tail interfollicular epidermis and hair follicles to transgene-negative littermates.
Keratin 15 (K15) and DNA label retention are markers of bulge stem cells (25, 32). No differences in K15 expression were observed between transgenic and non-transgenic epidermis examined in whole mount preparations of tail (Figure 3C). In addition, there were no differences in the number of label retaining cells, either within the hair follicles or interfollicular epidermis (Figure 3D).
As a further stem cell assay, we determined the colony forming efficiency of primary adult transgene-positive and -negative keratinocytes in culture (Figure 3D) (33). Whereas cells from non-transgenic and K14T188Iβ1 mice gave rise to a similar percentage of colonies, keratinocytes from K14WTβ1 mice had a lower ability to form colonies (Figure 3D).
To determine whether the T188Iβ1 integrin mutation influenced skin carcinogenesis, transgenic mice and their respective transgene-negative littermates were subjected to two-stage carcinogenesis with DMBA (to induce Ha-Ras mutations) and TPA (to promote tumour formation) (17) (Figure 4). Macroscopically, papillomas were identified as pedunculated or sessile mushroom-like lesions, while SCCs presented as ‘craters’ with signs of dermal ingrowth.
Papillomas first emerged in all groups between 7 and 11 weeks after the start of TPA promotion, and the maximum number of papillomas was reached by 20 weeks (Figure 4A, B and data not shown). No papillomas developed in mice treated with DMBA or TPA only (data not shown).
The proportion of mice that developed papillomas was not increased by expression of either transgene (29/50 for T188I versus 32/50 for NT; 46/50 for WT versus 50/50 for NT). However, both K14WTβ1 and K14T188Iβ1 transgenic mice developed significantly more papillomas than non-transgenic mice (Student’s t-test, p<0.0001) (Figure 4A, B).
In K14WTβ1 mice and non-transgenic littermates SCC first emerged between 16 and 20 weeks, reaching a plateau by 40 weeks (Figure 4C). There was no significant difference in the number of SCCs in K14WTβ1 transgenic and transgene-negative mice (Student’s t-test, p=0.5612). In addition, the wild-type transgene did not increase SCC incidence (29/50 for WTβ1; 36/50 for NT).
K14T188Iβ1 transgenic mice started to develop SCC three weeks earlier than non-transgenic and K14WTβ1 transgenic mice, exhibiting malignancies by week 16 after the start of TPA promotion (Figure 4D). Whereas both transgenes stimulated papilloma formation (Figure 4A, B), only K14T188Iβ1 transgenic mice developed more SCC than littermate controls (Student’s t-test, p=0.0093). The incidence of SCC was also higher in K14T188Iβ1 mice than in the NT controls (32/50 for T188Iβ1; 26/50 for NT).
The reproductive tract, liver, lung, spleen and lymph nodes of mice from the chemical carcinogenesis experiments were screened histologically for the presence of tumour cells. Both transgenes stimulated lymph node metastasis. In the K14T188Iβ1 group 14/50 mice developed metastases, whereas 8/50 littermate controls developed metastases. 13/50 K14WTβ1 mice developed metastases, compared to 8/50 controls.
Papillomas were scored as well or poorly differentiated on the basis of whether or not they contained a high proportion of cornified cells (Figure 5A, B). In well differentiated papillomas the boundary between the basal layer and the adjacent stroma was clearly defined, whereas in poorly differentiated papillomas there were often regions in which the basal cell layer invaded the stroma (Figure 5A). The basement membrane was intact in both categories of papillomas, but laminin deposition was more diffuse in the regions of basal layer disturbance (Figure 5A). At 20-30 weeks after DMBA treatment, the time when conversion to SCC occurs (Figure 4C, D), the proportion of well differentiated papillomas was significantly lower in K14T188Iβ1 mice (total number of papillomas examined: n=42 total) than in K14WTβ1 mice (n=44) and transgene-negative littermates (n=110) (Figure 4B; Pearson’s chi-square test).
In cultured keratinocytes integrin signalling through Erk/MAPK suppresses terminal differentiation (5, 34). To investigate whether Erk/MAPK signalling was influenced by the T188I mutant in vivo, we immunostained sections with an antibody to phosphoErk (pErk) (Figure 5C, D). Between 60% and 90% of the papillomas that developed in non-transgenic (total number of papillomas examined: n=152) and K14WTβ1 transgenic mice (n=68) were negative for pErk, while approximately 90% (n=43) of the T188Iβ1 papillomas were positive (Figure 5D; Pearson’s chi-square test).
All the SCCs from every tumour-bearing mouse in the chemical carcinogenesis experiments were assigned to one of four categories (Figure 6A), based on Broders’ classification (17). Undifferentiated tumours (spindle cell carcinomas) contained cells of fibroblastic morphology (Broders’ grade 4). Well (grade 1), moderately (grade 2) and poorly (grade 3) differentiated tumours had a decreasing proportion of differentiated cells (Figure 6A). In undifferentiated tumours there were proliferating, Ki67 positive, cells throughout the tumour mass (Figure 6B). There was also widespread proliferation in the poorly differentiated tumours (Figure 6B), whereas in the moderately and well differentiated tumours proliferation was confined to the cell layers closest to the tumour stroma (Figure 6B).
The frequency of undifferentiated (spindle) tumours was higher in K14WTβ1 transgenic (number of SCC analysed: n=24) and non-transgenic mice (n=50) than in K14T188Iβ1 transgenics (n=35) (Pearson’s chi-square test) (Figure 6C). In contrast, the frequency of poorly differentiated tumours was significantly higher in K14T188Iβ1 transgenics (Figure 6C).
Although the distribution of proliferating cells differed between the different tumour types (Figure 6B), the proportion of proliferating cells within the Ki67 positive regions (demarcated in Figure 6B) did not differ significantly between tumour types nor between transgenic and transgene-negative mice (Figure 6D). This suggests that the effect of the T188I mutation is primarily on tumour differentiation rather than on proliferation.
We have developed an in vivo model to examine the effect of a tumour-associated integrin. Expression of the T188I mutation did not affect normal skin architecture or homeostasis, but did increase the susceptibility of the epidermis to developing malignant tumours and also reduced tumour differentiation.
The transgenic human β1 integrins, were co-expressed with endogenous mouse β1 at the cell surface, were functional in mediating extracellular matrix adhesion, and had the same turnover time as the endogenous mouse β1 integrins. The T188I mutation enhanced Erk MAPK signalling and actin cytoskeletal assembly, and promoted cell spreading on low fibronectin concentrations to a greater extent than the wild-type subunit (20).
In comparison to transgene-negative mice, there was no change in proliferation and no evidence for any disruption of normal skin architecture or homeostasis in the K14WTβ1 and K14T188Iβ1 transgenics. This was unexpected because high integrin expression is an epidermal stem cell marker (2-4) and integrins regulate keratinocyte growth and differentiation (5, 20, 35-38). Thus whereas integrin-mediated adhesion is required for maintenance of the epidermal stem cell niche, β1 integrin activation is not sufficient to expand the stem cell compartment.
Expression of either the wild-type or mutant β1 transgene resulted in increased development of papillomas and increased lymph node metastases. This is consistent with reports that β1 integrin deletion impairs tumour initiation and maintenance (39). The positive effect of the transgenic integrins on papilloma development does not reflect simple overexpression of β1 integrins at the cell surface (Figure 2) (30). Instead it is likely to reflect the fact that the K14 promoter is not subject to the same negative regulation as the endogenous mouse β1 promoter (10, 24).
Three effects were selectively attributable to the T188I mutant integrin: more rapid conversion of papillomas to SCCs; a higher conversion frequency; and a higher proportion of poorly differentiated tumours. Expression of T188Iβ1 reduced differentiation in both the papillomas and SCCs, without affecting proliferation in the SCCs. This is consistent with the observation that the T188I mutation was found in a poorly differentiated SCC and that it has an impaired ability to trigger initiation of terminal differentiation of keratinocytes in culture (20).
One surprising effect of the T188I mutation was that it reduced the number of spindle cell tumours. These tumours are believed to arise from SCCs by a process of epithelial-mesenchymal transition (40). It is possible that this requires downregulation of extracellular matrix adhesion, which would be inhibited by the T188Iβ1 integrin transgene. The T188I mutation may prevent the changes in actin cytoskeletal assembly associated with spindle cell tumour formation (41). Alternatively, expression of the mutant integrin may decrease responsiveness to TGFβ (18, 19, 42, 43) or negatively regulate metalloproteinase expression (44), both of which are implicated in formation of spindle cell tumours.
K14T188Iβ1 papillomas had high levels of phosphoErk (Figure 5), which is likely to contribute to their reduced differentiation, and expression of T188Iβ1 enhanced Erk/MAPK signalling in vitro (Figure 2B; 5, 20). β1 integrin signalling through Erk/MAPK is associated with maintenance of the stem cell compartment in cultured human epidermis (5, 16, 34) and is linked to papilloma development in transgenic mice (16, 45). It is possible that activation of other signals, such as focal adhesion kinase (46), also contribute to the effect of T188I, although in cultured keratinocytes we have not observed a correlation between β1 integrin mediated adhesion and focal adhesion kinase activity (5).
Our data demonstrate that tumour-associated integrin mutations and polymorphisms have the potential to influence cancer susceptibility and disease outcome. While the tumour-associated integrin mutations are relatively rare, common integrin polymorphisms are associated with a range of other diseases, such as SLE (47, 48). Our studies indicate that it will be worthwhile to develop mouse models of additional integrin polymorphisms.
This work was supported by CR-UK; the Fundacão para a Ciência e Tecnologia (MF); and the Uehara Memorial Foundation (HF). We are deeply grateful to Ian Rosewell, Rob Rudling, Richard Poulsom, Will Howatt and other staff at the CR-UK London and Cambridge Research Institutes for advice and expert technical assistance. We acknowledge the support of the University of Cambridge and Hutchison Whampoa Ltd.