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Cas is a member of the focal adhesion complex. Phosphorylation of Cas by Src is an important event leading to cell transformation. Using mass spectrometry, we have mapped 11 sites in Cas that are phosphorylated by Src. These sites are all located between residues 132 and 414 of Cas, in a region that is required for binding to a number of other proteins including Crk. We tested synthetic peptides modeled on Cas phosphorylation sites, and found that the sequence containing tyrosine 253 was phosphorylated by Src most efficiently. Using cells derived from Cas-deficient mice, we confirmed that Cas greatly enhanced the ability of Src to transform cells. Phosphorylation of Cas on tyrosine 253 was not required for Src to increase growth rate, suppress contact inhibition, or suppress anchorage dependence. Yet, in contrast to these growth characteristics, phosphorylation of Cas on tyrosine 253 was required for Src to promote cell migration. Thus, a single phosphorylation site on this focal adhesion adaptor protein can effectively separate cell migration from other transformed growth characteristics.
Normal cells have intrinsic controls that limit their movement and growth, such as restraints imposed by cell cycle checkpoints. Cells must receive cues from their surrounding environment to override these restraints. Thus, cell growth normally relies on signals mediated from the extracellular matrix through integrins (1–3).
In contrast to normal cells, tumor cells ignore their surrounding environment, which allows them to overcome contact growth inhibition, lose anchorage dependence, and migrate to foreign tissues and organs. The degree to which tumor cells grow and migrate correlates with their aggressive potential (1, 2). Therefore, it is important to understand how extracellular signals guide cell behavior and how transformation ablates the need for integrin signaling.
Integrins transmit signals from the extracellular matrix to inside of the cell. Integrin signaling relies on a complex of associated kinases including focal adhesion kinase (FAK)1 and Src and adaptor proteins including Grb2, Shc, paxillin, and Cas (4, 5). Cas is an important component of the integrin signaling network (6). Cas was originally identified as a protein phosphorylated in v-src-transformed cells (7).
Cas has several structural motifs including an SH3 domain, proline-rich regions, and a cluster of tyrosine phosphorylation consensus sites that act as SH2 binding motifs (6, 8). FAK binds to the SH3 domain in the amino-terminal part of Cas (9–11), whereas Src binds to a proline-rich region and a phosphorylated tyrosine residue at the carboxyl end of Cas (12, 13). Although FAK may phosphorylate Cas in certain cases (14, 15), the biological activity of Cas depends on its phosphorylation by Src (16–18). After phosphorylation, Cas associates with a number of proteins, including Crk, Src, phosphatidylinositol 3-kinase, Nck, and phospholipase Cγ, via SH2 binding motifs (8, 10, 19).
Phosphorylation of Cas by Src plays a critical role in cell transformation (20, 21). For example, Src must phosphorylate Cas to promote anchorage-independent growth and cell migration (20–23). Therefore, understanding the mechanistic relationship between Cas and Src should help elucidate mechanisms that underlie fundamental aspects of tumor cell growth.
To better understand the role of Cas in cell transformation, we have identified residues that are phosphorylated by Src. We then examined the effects of these phosphorylation events on cell behavior. We report here that a single phosphorylation site on Cas, tyrosine 253, can effectively separate the effects of transformation on cell migration from other hallmarks of transformation including anchorage-independent growth.
Wild type Cas (8) and v-Src (24) were tagged at the amino terminus with polyhistidine and produced by the Bac-to-Bac Baculovirus Expression System (Invitrogen) as described (16). Briefly, cells were grown at 27 °C, infected with baculovirus expression vectors, collected and rinsed in phosphate-buffered saline by centrifugation, and lysed in a French pressure cell in lysis buffer (50 mM Tris-HCl, pH 8.5, 5 mM 2-mercaptoethanol, 100 mM KCl, 1 mM phenylmethylsulfonyl fluoride, and 1% Nonidet P-40 plus protease inhibitors). Lysates were clarified by centrifugation and applied to blue nickel-nitrilotriacetic acid resin to purify histidine-tagged Cas or Src according to the manufacturer’s protocols (Qiagen) as described (16).
A BamHI/NotI fragment containing Cas cDNA was subcloned into the complementary sites of the bacterial expression vector pET28A to produce the entire coding region of Cas with an amino-terminal polyhistidine tag as described by the manufacturer (Novagen). This construct was used as a template to produce site directed mutants with the QuikChange site-directed mutagenesis kit according to the manufacturer’s protocols (Stratagene), which were verified by sequencing on an ABI373 automated DNA sequencer as described (16). The tyrosine residue at position 253 was mutated to phenylalanine to produce CasY253F with the forward primer 5′-GCTCCAGGTTCCCAGGACATCTTTGATGTGCCCCCTGTTCG-3′ and a complementary reverse primer. The amino acids between residues 118 and 423 were deleted to produce Cas118Δ423. EcoRI sites were introduced at the nucleotides encoding amino acids 118 and 423 with forward primers 5′-CCCCAACCTGACAATGAATTCCTGGTACCCACTCCC-3′ and 5′-CCAGCCGAGCGAGAATTCCCAACAGATGGCAAGCGC-3′, respectively, and complementary reverse primers. The construct was religated after excising the resulting EcoRI fragment, which contains the entire substrate binding region of the protein. Wild type and mutant Cas proteins were produced in Escherichia coli strain BL21 DE3RP codon+ (Stratagene) and purified as done for Sf9 cells described above.
To examine the effects of Cas and Src on a blank background, fibroblasts from homozygous null Cas knockout cells were used as described previously (20, 21). The BamHI/NotI fragments encoding wild type Cas, CasY253F, or Cas118Δ423 were excised from pET28A vectors and subcloned into the BamHI/SnabI sites of pBABEhygro (25). An EcoRI/Hind3 fragment containing the entire coding cDNA region of the pp60 Src kinase of the Schmitt-Rupin strain of v-Src (26) was inserted between the EcoRI and SnabI sites of pBABEpuro (25). For controls, cells were transfected with empty vectors (pBABEhygro and/or pBABEpuro) as appropriate so that all transfectants were selected for hygromycin resistance and puromycin resistance conferred by the transfection vectors. All cells were transfected with equal concentrations of both plasmids (1 µg/well of 6-well plate), and clones were not taken from the resultant cells, thus avoiding potential consequences of clonal variation.
In vitro kinase reactions on full-length Cas proteins were performed as described previously (16). Basically, 1 µg of Cas protein was incubated at 30 °C in 10 µl of kinase buffer (10 mM Tris-HCl, pH 7.5, 20 mM MgCl2, 0.5 mM ATP) in the presence or absence of 0.15 µg of Src for varying lengths of time. After incubation with Src, some reactions were treated with 1 µg of Yersinia phosphatase for an additional 5 min. Reactions were stopped by the addition of SDS-PAGE sample buffer (to achieve a final concentration of 62.5 mM Tris-HCl, pH 6.8, 2% SDS, 10% glycerol, 50 mM dithiothreitol, 0.01% w/v bromphenol blue).
A continuous spectrophotometric assay was also used to measure kinase activity on synthetic peptides shown in Table II as described by Porter el al. (27). Reactions contained 100 mM Tris-HCl (pH 7.5), 10 mM MgCl2, 0.5 mM ATP, 1 mM phosphoenolpyruvate, 0.28 mM NADH, 89 units/ml pyruvate kinase, 124 units/ml lactate dehydrogenase, and varying concentrations of peptide substrates (75–2000 µM). The reactions were carried out in duplicate at 30 °C and were initiated by the addition of Src. Kinetic parameters were determined by fitting data to the Michaelis-Menten equation using nonlinear regression analysis of initial rates.
Protein (1 µg/lane) was resolved by SDS-PAGE and transferred to Immobilon-P membranes (Millipore). Antisera were used to detect p130 Cas (rabbit antiserum C-20, catalog no. 860, Santa Cruz Biotechnology) and tyrosine-phosphorylated proteins (P-Tyr-100 monoclonal, catalog no. 9411, Cell Signaling Technology). Reactions were detected by chemiluminescence with Amersham ECL plus as described (28, 29).
Western blot analysis was performed on cells grown for 24 or 72 h after plating. Cells were quickly aspirated, washed with phosphate-buffered saline, transferred to micro-centrifuge tubes, pelleted by a brief spin (1 min at 8000 × g), aspirated, lysed in SDS-PAGE sample buffer (2% SDS, 10% glycerol, 50 mM dithiothreitol, 0.01% bromphenol blue, and 62.5 mM tris-HCl (pH 6.8)), sheared through a 26-gauge needle, boiled for 5 min, and cooled on ice.
Protein (5 µg/lane) was resolved by SDS-PAGE and transferred to Immobilon-P membranes (Millipore). Antisera were used to detect p130 Cas (rabbit antiserum C-20, catalog no. 860, Santa Cruz Biotechnology.), total pp60v-Src kinase (anti-avian clone E10 monoclonal, catalog no. 05–185, Upstate Biotechnology), active pp60 kinase (rabbit antiserum specific for Src phosphorylated at Tyr416, catalog no. 2101, Cell Signaling Technology), total MAPK (rabbit antiserum against the p44 and p42 MAP kinase proteins, catalog no. 9102, Cell Signaling Technology), active MAPK (E10 monoclonal antibody specific for p42 and p44 MAP kinase protein phosphorylated at Thr202 and Tyr204, catalog no. 9106, Cell Signaling Technology), other proteins phosphorylated on tyrosine residues (P-Tyr-100 monoclonal, catalog no. 9411, Cell Signaling Technology), and β-actin (monoclonal antibody AC15, catalog no. A5441, Sigma). Reactions were detected by chemiluminescence with Amersham ECL plus as described (28, 29).
Crk was immunoprecipitated to evaluate its association with wild type Cas and CasY253F in mammalian cells as described by Klemke et al. (23). Cells were washed twice with phosphate-buffered saline, lysed with a solution containing 50 mM Tris pH 7.5, 150 mM NaCl, 5 mM EDTA, 1 mM sodium vanadate, protease inhibitor mixture (Sigma, P8340), and 1% Nonidet P-40, and clarified by centrifugation. 4 mg of total protein was precleared with protein G-Sepharose 4 Fast Flow beads (Amersham Biosciences, catalog no. 17-0618-01), incubated over-night with monoclonal antibody against Crk (Transduction Laboratories, catalog no. 610035), immunoprecipitated with protein G-Sepharose beads, eluted in SDS-PAGE sample buffer, resolved by gel electrophoresis, and analyzed by Western blotting with antiserum against Crk and Cas as described above.
Cas protein (1 µg) produced by Sf9 cells was subjected to in an in vitro kinase reaction for 1 h either in the presence of 0.5 mM ATP alone or with ATP plus 0.15 µg of purified v-Src. Cas was then resolved by SDS-PAGE, and examined by MALDI-TOF MS as described previously (28). Briefly, protein was detected by Coomassie staining, excised, rehydrated, washed with 50 mM Tris (pH 8.0), 50% acetonitrile, dried, and completely digested with trypsin in 25 mM Tris (pH 8.5). Peptides were then extracted with 50% acetonitrile, 0.1% trifluoroacetate, dried, suspended in 10 mg/ml 4-hydroxy-α-cyanocinnamic acid in 50% acetonitrile, 0.1% trifluoroacetate containing bovine insulin and human angiotensin as internal standards, and applied to a MALDI sample plate. MALDI mass spectrometric analysis was performed on a PerSeptive Voyager DE-RP mass spectrometer in the linear mode. Profiles were queried against the expected Cas peptide products, and phosphorylated residues were apparent by an increase in molecular mass of 80 daltons (relative to the Cas + ATP samples).
Protein bands were subjected to in-gel digestion as for MALDI-MS. Peptide extracts were desalted using a C18 ZipTip (Millipore) followed by elution from the tip with 10 ml of 50% acetonitrile. Immediately prior to injection the acetonitrile was removed on a Speed-vac concentrator, and the volume was brought to ~2 ml. Analysis was done on a Micromass Q-Tof hybrid quadrupole/time-of-flight mass spectrometer with a nanoelectrospray source. A fused silica tip mounting adapter from New Objective was fitted with a 75-mm inner dimension fused silica tip, also from New Objective, connected through 50-mm inner dimension fused silica tubing to the LC detector outlet. Nano-LC was performed with an LC Packings Ultimate micro pump and solvent organizer, and an Ultimate detector with a 10-nl flow cell and 214-nm wavelength. Sample was resolved through an LC Packings C18 PepMap column (5 mm, 75-mm ID, 15-cm length) at a flow rate of 200 nl/min and an injection volume of 1ml (Solvent A: 2% acetonitrile, 0.1% formic acid; Solvent B: 80% acetonitrile, 0.1% formic acid; loading solvent: 0.1% formic acid).
For all assays, cells were grown in Dulbecco’s modified Eagle’s medium + 10% fetal bovine serum at 37 °C in 100% humidity. All comparisons were done in parallel to avoid any changes in culture conditions between experiments. 20,000 cells were seeded in 1 ml in each well of tissue culture-treated 12-well cluster plates (Falcon, catalog no. 3043) to examine anchored growth or in ultra low attachment 24-well cluster plates (Corning, catalog no. 3473) to examine nonanchored growth. Cell numbers were obtained by Coulter counter at the time points indicated in the Fig. 7.
To examine cell migration, 200,000 cells were plated in 6-well cluster plates on cell culture inserts with a 3-µm pore size as directed by the manufacturer (Transwell clear, Costar) and grown for 72 h. Cells were then separately released from the top of the membrane, the bottom of the membrane, and well beneath the membrane. Migration was then quantitated as the percent of cells found in the well over the total cell number.
Src and Cas were purified from Sf9 cells and utilized for in vitro kinase assays. Phosphorylation of Cas by Src was evident in these experiments. The apparent molecular mass of Cas was shifted by Src phosphorylation from 130 to 170 kDa in SDS-polyacryl-amide gels. This effect was reversed by treatment with a tyrosine phosphatase (Fig. 1).
To identify sites phosphorylated by Src, Cas was incubated with Src and ATP or with ATP alone, resolved by SDS-PAGE, cleaved with trypsin, and analyzed by MALDI-TOF MS. As shown in Fig. 2, several tryptic fragments were found in the unphosphorylated state in the ATP-treated sample, but these were shifted by the mass of a phosphate (+80) in the Src-phosphorylated sample. Based on these data, 11 tyrosine residues (132, 169, 183, 196, 238, 253, 271, 291, 301, 391, and 414) were phosphorylated by Src (Table I).
Quantitative kinase assays were performed on peptides harboring several of the phosphorylation sites identified by MALDI-TOF MS. As shown in Table II, the peptide based on tyrosine 253 was the most efficient substrate of those tested, in terms of kcat/Km. Although individual sites might be phosphorylated differently in the context of the folded three-dimensional structure of Cas, the mass spectrometry and peptide data collectively point to tyrosine 253 on Cas as a primary target of Src phosphorylation.
Phosphorylation of full-length Cas on tyrosine 253 by Src was verified by LC-MS-MS. The calculated mass of the peptide sequence between residues 243 and 259 (HLLAPGSQDIYDVPPVR) is 1877 daltons. Phosphorylation of tyrosine 253 increased the mass of this fragment by 80 daltons to 1957 daltons (Fig. 2 and Table I). The carboxyl-terminal portion of this fragment, containing tyrosine 253, was clearly detected by LC-MS-MS in Fig. 3. The pattern of fragment ions confirmed the presence of phosphorylated tyrosine 253, with a mass of 243 daltons.
The phosphorylation sites identified in this study were all located between amino acids 132 and 414 of Cas. Expression vectors were created to produce full-length wild type Cas, a site mutant with tyrosine 253 changed to phenylalanine (Y253F), or a deletion mutant missing the entire substrate for Src substrate region between amino acids 118 and 423 (118Δ423). As shown in Fig. 4, wild type Cas and CasY253F were both phosphorylated by Src in vitro, whereas Cas118Δ423 was not. Thus, Src phosphorylated Cas at sites in addition to tyrosine 253, but they all resided within the Src substrate region as presented in Fig. 5.
Wild type Cas and mutant Cas constructs shown in Fig. 5 were transfected into fibroblasts derived from homozygous null Cas knockout mice to examine their effects on cell transformation by v-Src. However, in agreement with recent reports (21, 30, 31), we found Cas118Δ423 to be extremely toxic to mammalian cells. This construct appeared to cause rapid apoptosis, and we were unable to obtain stable transfectants for further study. Nonetheless, we were able to proceed with wild type Cas and CasY253F.
As shown in Fig. 6, Src transfection caused cells to assume a spindly morphology compared with Cas or control transfectants. In contrast, coexpression of Cas and Src caused cells to assume a refractive and rounded morphology typical of transformed cells. Wild type Cas and CasY253F were indistinguishable in their ability to support Src-induced transformation (Fig. 6).
Eventually, Cas and control transfectants formed contact inhibited monolayers. At higher densities, cells transfected with Src formed multilayered foci. However, expression of Cas appeared to augment foci formation of postconfluent Src-transfected cells (Fig. 6).
Foci formation of Src transfectants suggested a loss of contact growth inhibition. This was made evident by growth curves shown in Fig. 7. Control transfectants achieved an average saturation density of less than 1200 cells mm2. Cas transfectants surpassed this by about 50%, reaching an average density of nearly 1800 cells/mm2. Transfection with Src increased saturation density of these cells by about 300% to over 3000 cells/mm2 or about 6-fold higher than the increase caused by Cas. Wild type Cas did not further increase the saturation density of Src transfectants. However, Cas did enable the Src-transfected cells to reach higher densities faster (in 11 days as opposed to 15 days). The same was true for CasY253F, which enabled cells to reach an even higher saturation density of over 3700 cells/mm2 in the same amount of time (11 days). Thus, wild type Cas and CasY253F both augmented the ability of Src to decrease contact growth inhibition of these cells.
Cas also enabled Src to increase the growth rate of these cells. Control transfectants displayed a log phase doubling time of 24 h. Cells transfected by either Cas or Src alone displayed a similar log phase doubling time of 23 h. In contrast, cells transfected with both Cas and Src displayed a faster log phase doubling time of just 16 h. Thus, Cas potentiated the ability of Src to increase cell growth rate, as well as to suppress contact growth inhibition.
Loss of anchorage dependence is a reliable hallmark of most tumor cells (3, 32). Consistent with earlier reports (20, 21), Cas augmented the ability of Src to promote anchorage-independent growth. As shown in Fig. 7, cells transfected with Cas or control vectors could not grow in suspension, whereas 200 Src transfectants grew to about 8500 in 11 days. In contrast, 200 Src transfectants expressing wild type Cas or CasY253F grew to an average of over 37,000 or 55,000, respectively, in the same period of time. This was significantly better than cells transfected with Src alone (p < 0.005 by t test). Thus, wild type Cas and CasY253F both potentiated the ability of Src to override anchorage dependence.
In addition to promoting anchorage-independent growth of transformed cells, Cas plays an important role in process of cell migration (21). As shown in Fig. 7, less than 0.5% of the cells transfected with control vectors, Cas, or Src were able to migrate through pores in a migration chamber. In contrast, more than 8% of cells transfected with both Src and wild type Cas migrated, representing a significant increase over cells transfected with Src alone (p = 0.0001 by t test). However, less than 2% of cells transfected with both Src and CasY253F migrated, representing a 4-fold decrease compared with Src-transformed cells expressing wild type Cas. Therefore, wild type Cas enabled Src transformed cells to migrate significantly better than CasY253F (p = 0.0003 by t test).
We examined the effects of wild type Cas and CasY253F on Src activity in these cells. Consistent with previous reports (20), Cas did not affect v-Src activity (Cas has previously been shown to activate c-Src, the down-regulated cellular form of Src (16, 33)). As shown in Fig. 8, all cells transfected with Src had similar levels of total and active forms of the kinase. Therefore, Cas is likely to affect Src signaling downstream of its intrinsic kinase activity.
Previous reports indicate that binding of Crk to Cas is important for cell migration (21–23). Therefore, we investigated the ability of CasY253F to associate with Crk. As shown in Fig. 9, both wild type and mutant Cas associated with Crk in Src transformed cells.
Cas plays a critical role in cell growth and transformation (6). The importance of Cas in cell transformation is highlighted by investigations into the relationship between Cas and Src. For example, experiments with site-directed mutants revealed that the ability of Src and Crk to transform cells relies on their ability to bind Cas (34, 35). In addition, ablation of Cas with antisense constructs curtailed transformed characteristics imparted by agents including v-Src (36).
We identified 11 Src phosphorylation sites on Cas. These were all within the Src substrate region between amino acids 118 and 423 of Cas. These data are consistent with reports that sites outside of this region (e.g. tyrosine residues 668 and 670) are not phosphorylated by Src (37). These data are also consistent with reports that Src must phosphorylate tyrosine residues in this region to transform cells (21).
Our results also confirm reports that deletion of the Src substrate region causes Cas to induce cellular apoptosis (30). An apoptotic role for Cas may also be inferred from its cleavage by caspase-3 (38). However, mechanisms by which ablation of the Src substrate region turns Cas apoptotic are intriguing. In the absence of Cas (e.g. in Cas knockout cells), its homologues HEF1 and Efs/Sin may perform scaffolding functions needed for cell survival (6). HEF1 and Efs/Sin may not completely substitute for Cas because Cas knockout mice suffer from severe developmental disorders. However, some of this deficiency may be due to differences in expression patterns as opposed to function (20). Also, Cas is not required for formation of focal adhesions (20), whereas HEF1 is found in focal adhesion plaques of adherent cells (39). Therefore, deletion of the Src substrate region may cause Cas to act as a dominant negative protein that interferes with itself and its homologues, thus causing events leading to apoptosis. Nonetheless, the case does not seem simple because, instead of blocking apoptosis, transfection of HEF1 can actually increase apoptosis in some mammary carcinoma cells (39).
Regardless of how the Src substrate region in Cas affects apoptosis, the importance of its phosphorylation by Src in cell transformation is clear (20, 21). Our data confirm this in that Cas significantly enhanced the ability of Src to cause morphological transformation (Fig. 6). More importantly, Cas significantly increased the ability of Src to decrease contact growth inhibition and to increase anchorage-independent growth (Fig. 7).
Our data indicate that Src phosphorylates 11 sites within the Src substrate region of Cas. Once these sites are phosphorylated, they can bind to SH2 domains on different proteins (6). Tyrosine 253 was a preferred Src phosphorylation site in Cas. However, phosphorylation of this site was not required for Src to block contact growth inhibition or anchorage dependence. Instead, phosphorylation of tyrosine 253 was required for Src to augment the migration of transformed cells. Therefore, this site may target individual proteins to focal adhesions that are specifically required for cell migration to occur.
Binding of Crk to the Src substrate region of Cas is required for cell migration and invasion into collagen (21–23). In addition, Huang et al. (21) have recently reported that phosphorylation of this region is required for Crk binding to Cas, and for Src to induce cell migration but not for Src to promote nonanchored cell growth. Also, Cho and Klemke (40) have recently demonstrated that the association of Cas with Crk activates the small GTPase Rac1 to direct cell movement by causing the growth and retraction of pseudopodia. This same Cas/Crk/Rac1 association also blocks apoptosis (22, 23). However, Cas may regulate the binding of Crk to other proteins including Gab, Cbl, and the insulin receptor substrate IRS1 (41–43), which have all been implicated in cell migration (44–46).
Phosphorylation of Cas during cell migration differs from its phosphorylation profile during cell division. Cas is phosphorylated on serine and threonine, whereas tyrosine residues are dephosphorylated during mitosis (47). As opposed to the Cas/Crk/Rac1 cascade implicated in cell migration, phosphorylation of Cas at sites other than tyrosine 253 may enable Grb2 to associate with Shc and Shp2 to activate the Ras/MAPK cascade, which then activates genes required for mitogenesis via serum response elements (48).
Taken together, because phosphorylation of tyrosine 253 is not required for the effects of Cas on cell growth and anchorage independence but is required for Cas to enhance transformed cell migration, it may be proposed that phosphorylation of this site is especially suited to activate Rac, whereas other sites enable the activation of Ras. This system provides a striking example of how a single phosphorylation site on one protein can determine whether or not a tumor cell will migrate. Ultimately, this situation may be exploited to precisely target specific aspects of tumor cell growth, such as metastasis, without inhibiting the processes required for normal cell behavior.
We are very grateful to Drs. Amy Bouton (University of Virginia) and Hisamaru Hirai (University of Tokyo) who graciously supplied Cas knockout cells, Hyunna Song for kinetic experiments of Cas peptides, and Dr. Jim Bliska (State University of New York at Stony Brook) for helpful discussions.
*This research was funded in part by National Institutes of Health Grants CA58530 (to W. T. M.) and CA88805-01A2 (to G. S. G.), and a grant-in-aid and research fellowship from the Foundation for the Promotion of Cancer Research, part of the Second Term Comprehensive 10-Year Strategy for Cancer Control, from the Japanese Ministry of Health and Welfare (to G. S. G.).
1The abbreviations used are: FAK, focal adhesion kinase; SH2 and SH3, Src homology 2 and Src homology 3, respectively; MALDI-TOF, matrix-assisted laser desorption ionization/time-of-flight; MS, mass spectrometry; LC-MS-MS, liquid chromatography-tandem mass spectrometry; MAP, mitogen-activated protein; MAPK, MAP kinase.