Muscarinic receptor agonist-induced βPix binding to β-catenin promotes colon neoplasia

M3 muscarinic receptors (M3R) modulate β-catenin signaling and colon neoplasia. CDC42/RAC guanine nucleotide exchange factor, βPix, binds to β-catenin in colon cancer cells, augmenting β-catenin transcriptional activity. Using in silico, in vitro, and in vivo approaches, we explored whether these actions are regulated by M3R. At the invasive fronts of murine and human colon cancers, we detected co-localized nuclear expression of βPix and β-catenin in stem cells overexpressing M3R. Using immunohistochemistry, immunoprecipitation, proximity ligand, and fluorescent cell sorting assays in human tissues and established and primary human colon cancer cell cultures, we detected time-dependent M3R agonist-induced cytoplasmic and nuclear association of βPix with β-catenin. βPix knockdown attenuated M3R agonist-induced human colon cancer cell proliferation, migration, invasion, and expression of PTGS2, the gene encoding cyclooxygenase-2, a key player in colon neoplasia. Overexpressing βPix dose-dependently augmented β-catenin binding to the transcription factor TCF4. In a murine model of sporadic colon cancer, advanced neoplasia was attenuated in conditional knockout mice with intestinal epithelial cell deficiency of βPix. Expression levels of β-catenin target genes and proteins relevant to colon neoplasia, including c-Myc and Ptgs2, were reduced in colon tumors from βPix-deficient conditional knockout mice. Targeting the M3R/βPix/β-catenin axis may have therapeutic potential.


Results βPix and β-catenin colocalize in nuclei of colon cancer cells overexpressing M 3 R
Normal and neoplastic colon epithelial cells express a mix of M 1 R and M 3 R 39 .Thus, we initially explored differences in the relative expression and distribution of M 1 R and M 3 R in human colon cancer and compared this to the expression pattern of βPix (Fig. 1).Using anti-MR antibodies we 5,40 and others 41 previously used for IHC, we compared M 3 R to M 1 R expression in surgical specimens of sporadic colon cancer by immunohistochemistry (IHC).As recommended by Jositsch et al. 42 , we validated anti-M 1 R and anti-M 3 R antibody specificity using tissues from wild-type, M 1 R-, M 3 R-, and dual M 1 R/M 3 R-deficient mice (Supplemental Fig. 1a).We used these validated MR-selective antibodies to compare M 1 R and M 3 R expression in tissue samples from human normal colon epithelium (Supplemental Fig. 1b,c) and colon adenocarcinomas (Fig. 1).In sections from the normal human colon, we observed equivalent epithelial cell staining for M 1 R and M 3 R (Supplemental Fig. 1b,c).In contrast, at the tumor invasive front, CD133-positive colon cancer stem cells, clustered around blood vessels, demonstrated intense M 3 R but not M 1 R staining (Fig. 1a, top panels).The use of CD133, one of the first identified colon cancer stem markers, for this purpose has been validated by many investigators 43 .In the same areas demonstrating intense M 3 R staining, we detected nuclear co-localized βPix and β-catenin staining (Fig. 1b).Our findings that M 3 R but not M 1 R were overexpressed in colon cancer stem cells with colocalized overexpression of βPix and β-catenin are compatible with our hypothesis that M 3 R regulate the interaction between βPix and β-catenin, and hint at its functional importance.

CHRM3/M 3 R and ARHGEF7/βPix are overexpressed in colon cancer
We examined the relationship between CHRM3/M 3 R and ARHGEF7/βPix expression in colon cancer.CHRM3/ M 3 R is overexpressed in 60-80% of colon cancers [3][4][5] .Lei et al. reported ARHGEF7/βPix overexpression in colon cancer cell lines and in a small set of tissues; ARHGEF7 expression levels were significantly increased in advanced stage colorectal cancer (TNM stage III) compared to early-stage disease (TNM stage I/II) 36 .Thus, ARHGEF7/ βPix and CHRM3/M 3 R appear to share expression patterns in progressive colon neoplasia.
To confirm that ARHGEF7 and CHRM3 mRNA levels are increased in cancer compared to normal colon, we interrogated publicly available databases; Oncomine 44 , Gene Expression Profiling Interactive Analysis 45 , Human Protein Atlas 46 , and the UALCAN server 47 .Per Oncomine, in 12 datasets ARHGEF7 mRNA transcripts are overexpressed 2.640-fold in cancer compared to normal colon (p = 6.05E-12) 44,48 .CHRM3 mRNA transcripts are overexpressed 2.411-fold in cancer compared to normal colon (p = 3.81E-15) 44,48 .CHRM3 and ARHGEF7 are in the top 10% overexpressed colon cancer genes 44,48 .
We compared the subcellular distribution of βPix in 29 paired colon cancers and normal colon, and its correlation with M 3 R expression (Fig. 2e).IHC staining intensity was scored in 0.5 increments from 0 to 3.5 by a senior pathologist masked to the purpose of the analysis.Nuclear βPix staining was 2.5-fold greater in cancer.Likewise, M 3 R staining was increased in cancer (Fig. 2f).M 3 R expression correlated with nuclear βPix staining (r 2 = 0.44; p < 0.05), and both βPix and M 3 R immunostaining were more intense in cancer compared to normal tissue (Fig. 2g).

MR activation stimulates cytosolic and nuclear βPix binding to β-catenin
In established and primary human colon cancer cell cultures, we explored whether MR activation augmented βPix/β-catenin binding.In cytosolic and nuclear fractions from HT-29 and H508 cells that overexpress M 3 R and have mutated and wild-type APC, respectively 51 , we assessed binding of endogenous βPix to β-catenin.We used an antibody directed against the βPix SH3 domain to precipitate βPix followed by immunoblotting extracts with anti-β-catenin and anti-βPix antibodies (Fig. 3a/b) and reversed the sequence by immunoprecipitating β-catenin and immunoblotting for βPix and β-catenin (Fig. 3c/d).In acetylcholine (ACh)-treated HT-29 cells, we detected   increased cytosolic binding of βPix to β-catenin (maximal by 5 min; Fig. 3a/c), followed by increased nuclear binding of βPix to β-catenin (maximal by 10 min; Fig. 3b/d).The actions of ACh were blocked by atropine (Fig. 3e/f).We duplicated these results in a second colon cancer cell line using a different MR agonist.Treating either HT-29 or H508 colon cancer cells with carbamylcholine (carbachol) induced two-to four-fold increased βPix binding to β-catenin (Fig. 3 g/h).
Post-M 3 R signal transduction is mediated by kinase-dependent mechanisms involving activation of PKC-α and/or transactivation of EGFR with downstream activation of the mitogen-activated protein kinase (MAPK)/ ERK pathway; there is extensive crosstalk between signaling pathways 52 .To explore post-receptor signaling underlying MR agonist-induced nuclear binding of βPix to β-catenin, we used previously validated chemical inhibitors 52 .Pre-treating HT-29 cells with Gö6976, a PKC inhibitor, or with AG-1478, an EGFR inhibitor, nearly abolished MR agonist-induced binding of βPix to β-catenin (Fig. 3i).To confirm PKC and EGFR activation play a role in MR agonist-induced binding of βPix to β-catenin, we treated HT-29 colon cancer cells with phorbol 12-myristate, 13-acetate (PMA), a selective PKC activator and epidermal growth factor (EGF).PMA induced robust binding of endogenous βPix to β-catenin, an action inhibited by Gö6976 (Fig. 3j, left).EGF had a more modest effect on the binding of endogenous βPix to β-catenin (Fig. 3j, right).We concluded that post-MR signaling primarily via PKC, most likely PKC-α 52 , activation, but also via EGFR activation mediate MR agonist-induced binding of βPix to β-catenin.To validate these findings, we used different experimental approaches with cells from fresh primary adenocarcinomas and established cell lines.In cytosolic extracts from primary colon cancer cells treated with carbachol we detected robust βPix binding to β-catenin (Fig. 4a).Quantitative measurements of cytosolic fractions revealed that carbachol stimulated three-to tenfold increases in anti-βPix antibody band density (Fig. 4b), supporting the clinical relevance of our findings with established cell lines.Our ability to detect nuclear βPix binding to β-catenin in primary cells was compromised by sluggish in vitro cell proliferation and cell-to-cell variation.To circumvent technical difficulties in assessing MR agonist-induced nuclear binding of βPix to β-catenin in primary www.nature.com/scientificreports/colon cancer cells, we employed immunofluorescence (IF) microscopy, proximity ligation assays (PLA) 53 , and a novel approach combining fluorescence microscopy with flow cytometry 54 .Using primary colon cancer cells and IF microscopy (Fig. 4c, left), we detected modest constitutive cytoplasmic colocalization of βPix and activated β-catenin (ABC), using an antibody that recognizes activated β-catenin unphosphorylated at Ser-37 and Thr-41 residues 55 .Treating primary colon cancer cells with ACh stimulated striking cytoplasmic and nuclear colocalization of βPix and activated β-catenin (Fig. 4c, right; arrows indicate nuclear co-localized βPix and activated β-catenin).
We used PLA which detects proteins colocalized within 40 nm 53 , as another test of MR agonist-induced nuclear co-localization of βPix and β-catenin.Applying PLA to two fresh colon cancer preparations, we identified robust MR agonist-induced nuclear signals consistent with colocalized βPix and β-catenin (representative nuclei shown in Fig. 4d), actions blocked by atropine (not shown).
The 5-min time lag between MR agonist-induced βPix binding to β-catenin in the cytoplasm and the nucleus could represent delayed nuclear translocation of βPix, β-catenin, or the βPix/β-catenin complex.Alternatively, it could result from delayed nuclear translocation of signaling molecules (e.g., PKCα).We used fluorescence cell sorting to explore if MR activation stimulated nuclear translocation of βPix or β-catenin.After treating HT29 cells with 200 µM ACh for 10 min, we measured shifts in nuclear localization of total β-catenin, activated β-catenin, and βPix.We failed to detect an increased nuclear signal for either total or activated β-catenin (Fig. 4e, left and middle).In contrast, in ACh-treated cells we observed a modest nuclear signal for βPix that was abolished by atropine (Fig. 4e, right).To assess overall changes in nuclear localization, we used the 'similarity score' to measure the change in similarity between protein and nuclear images (Fig. 4f).Post MR agonist treatment, median similarity scores showed no significant changes in nuclear localization of total or activated β-catenin (Fig. 4f, left and middle panels; Table 1).As shown in Fig. 4f (right), compared to control, there was a rightward shift in βPix similarity scores, abolished by pretreating cells with atropine.Nonetheless, these changes representing only a 4% change in nuclear signal intensity were unlikely to be biologically meaningful and did not achieve statistical significance (Table 1).
Collectively, our findings suggest M 3 R agonists stimulate binding of pre-existing nuclear βPix to β-catenin and not cytoplasm-to-nucleus translocation of either βPix or β-catenin.Thus, our working model suggests M 3 R activation stimulates βPix binding to β-catenin independently within the cytoplasm and nucleus.We performed a pilot experiment to test whether nuclear βPix bound to β-catenin could participate as a TCF-4 transcriptional cofactor.We used anti-TCF-4 antibodies to determine whether exogenous Flag-tagged βPix augmented β-catenin binding to TCF-4.Immunoprecipitation assays using nuclear extracts derived from HCT116 colon cancer cells incubated with increasing concentrations of Flag-βPix revealed progressively augmented Flag-βPix and β-catenin binding to TCF-4 (Fig. 4h).These results suggest a mechanism whereby MR-stimulated nuclear binding of βPix to β-catenin can alter gene expression and cell function.

βPix deficiency attenuates MR agonist-induced changes in cell function
Lei et al. reported that up-and down-regulating βPix expression in HCT116 and Lovo human colon cancer cell lines, respectively augmented and attenuated cell migration and invasion 36 .MR activation also stimulates cell migration 6 and invasion 7,52 .Hence, we next examined whether transient and stable βPix deficiency alters MR agonist-induced cell proliferation, migration, and invasion.
We next examined c-Myc, β-catenin, and Cox2 protein expression in normal colon and tumors harvested from six Arhgef7 CKO and six control mice.Whereas β-actin loading controls were similar in gels from control and CKO mice, except for Cox2 signals in CKO mice 2 and 4, expression of colon cancer-related proteins was substantially reduced in βPix-deficient adenocarcinomas (Fig. 6g).CKO mouse number 2 was the same mouse with the 'outlier' Ptgs2 mRNA signal (Fig. 6f).We confirmed mouse genotypes, so we cannot presently explain how mice 2 and 4 escaped downregulated Cox2 expression observed with βPix deficiency in other mice.
Lastly, we sought an association between ARHGEF7 and PTGS2 expression in colon cancer.Using methods described previously 57 , we interrogated public gene databases for paired normal colon and cancer (n = 78 for

Discussion
There is growing interest in noncanonical roles for GTP-binding proteins that modulate post-receptor signaling.Such interactions fine-tune signaling that might result in unbridled cell proliferation and other attributes of neoplasia.ARHGEF6 and ARHGEF7, encode two proteins, αPix and βPix, respectively, that interact functionally with many molecules [reviewed in 58 ].Of more than 40 'proven' βPix binding interactions with oligomeric protein partners [Table S1 in 58 ], complexes between βPix and the Src family of protein tyrosine kinases, GPCRkinase-interacting proteins, EGFR, and β-catenin are likely most relevant to colorectal neoplasia.Yet, despite the potential biological and pathological consequences of βPix-binding interactions, little was known regarding how these interactions are regulated.
Previously, we uncovered a noncanonical role for βPix, wherein its binding to β-catenin regulates transcriptional activity and cell function 38 .Here, we provide evidence that M 3 R activation regulates this interaction.In addition to demonstrating that CHRM3/M 3 R and ARHGEF7/βPix are coordinately overexpressed in colon cancer, immunoprecipitation experiments revealed that in the cytosol and nucleus M 3 R activation provokes timedependent βPix binding to β-catenin by a PKC-dependent mechanism.Crucially, the validify of these findings were strengthened by multiple lines of evidence from IF microscopy, PLA, and fluorescence cell sorting assays.Although the data shown in Fig. 1 suggest nuclear colocalization of βPix and β-catenin is exaggerated in colon cancer stem cells, the results of experiments shown in Fig. 4c,d,e and g, clearly demonstrate this also occurs in the general population of colon cancer cells − it is not limited to colon cancer stem cells.Pilot data suggested nuclear βPix may be a cofactor in the β-catenin/TCF4 transcription factor complex, thereby regulating β-catenin target gene expression.Supporting the functional importance of MR agonist-induced βPix binding to β-catenin, we found that reducing βPix expression in vitro attenuated M 3 R agonist-induced colon cancer cell proliferation, migration, and invasion.Moreover, in the AOM/DSS murine model of colon cancer, mice with conditional intestinal epithelial cell βPix deficiency 59 had significantly fewer colon tumors, primarily fewer adenocarcinomas, a finding exaggerated in animals treated with a MR agonist.
In human colon cancer cells, we observed that βPix knockdown reduced PTGS2 expression.The expression of PTGS2, whose protein product, cyclooxygenase-2 (COX2), catalyzes the metabolism of arachidonic acid to prostaglandins and other bioactive molecules, must be carefully regulated.Elevated levels of COX2 are associated with the development and progression of colon neoplasia [60][61][62] and reduced survival 63 ; in both animal models and humans, inhibiting COX-2 activity with non-steroid anti-inflammatory drugs attenuates colon neoplasia.MR activation in human colon cancer cells up-regulates COX2 expression 4 .We found Ptgs2 expression was also greatly reduced in tumors from Arhgef7 CKO mice with intestinal epithelial cell-selective βPix deficiency.Finding a connection between the M 3 R/βPix/β-catenin and COX2 expression provides a mechanistic framework that may be clinically relevant.Indeed, the lack of a relationship between ARHGEF7 and PTGS2 expression in colon cancer suggests M 3 R activation is pivotal to augmenting COX2 expression by a βPix-dependent mechanism.
Based on the current findings, we propose a model wherein post-MR signal transduction, mediated primarily by PKC-α activation, stimulates βPix binding to β-catenin in the cytoplasm and nucleus.Our preliminary data suggest nuclear βPix binds β-catenin/TCF4 transcription complexes, augmenting key β-catenin target gene expression, e.g., PTGS2, important for cancer progression [60][61][62] .Reduced βPix expression attenuates β-catenin target gene expression, cell function, and murine colon tumor formation.Nonetheless, we acknowledge that our work has limitations.In vitro cell models may not recapitulate complex in vivo interactions and murine cancer models, while mimicking key features of human colon cancer progression, do not fully mirror the development and progression of human colon neoplasia.Lastly, a putative role for βPix as a cofactor in the β-catenin/TCF4 transcription factor complex must remain speculative until confirmed by complementary approaches.Pursuing this intriguing finding and confirming a functional interaction between endogenous βPix and the β-catenin/ TCF-4 transcription factor complex that alters β-catenin target gene expression requires luciferase reporter, electrophoretic mobility shift, chromatin immunoprecipitation, and other approaches beyond the scope of the current project and will be pursued in future work.
In conclusion, our findings identify a noncanonical role of βPix as an intermediary between M 3 R and β-catenin signaling that modulates colon cancer gene expression and cell function.Employing rigorous in vitro and in vivo experimental designs to test established human colon cancer cell lines and fresh human colon cancer cells using complementary innovative approaches, we uniformly observed M 3 R agonist-stimulated βPix/β-catenin binding in both the cytosolic and nuclear compartments and consistent effects on downstream expression of β-catenin target genes.Targeting the M 3 R/βPix/β-catenin axis has therapeutic potential.Our experience using Arhgef7 CKO mice with intestinal epithelial cell-selective βPix deficiency suggests targeting intestinal βPix would be safe; Arhgef7 CKO mice are healthy and fertile with modest phenotypic changes 59 .Lastly, since other upstream receptors act through PKC-α, our findings may be mechanistically relevant to other receptors and signaling pathways in colon neoplasia and other cancers in which muscarinic receptor signaling plays a prominent role.

Animals
We created Arhgef7 flox/flox -/Tg(Villin-Cre) mice (Arhgef7 CKO mice) with intestinal epithelial βPix deficiency 59 .Mice were bred, housed, and treated under identical conditions in a pathogen-free room.To achieve microbiome equivalence, we co-housed animals throughout these studies until they were euthanized.Experiments were approved by the Institutional Animal Care and Use Committee of the University of Maryland, Baltimore, and VA Maryland Health Care System Research and Development Committee.All experiments were performed in accordance with institutional guidelines and regulations and the authors complied with the ARRIVE guidelines.

Established human colon cancer cell lines
HT-29, H508, SNU-C4, and HCT116 human colon cancer cell lines were authenticated and purchased from American Type Culture Collection.HT-29 and HCT116 cells were grown in McCoy's 5A medium and H508 and SNU-C4 wells were grown in RPMI 1640 (Life Technologies-Thermo Fisher), both supplemented with 10% FBS.Cells were grown at 37ºC, with 5% CO 2 in a humidified incubator and passaged weekly at subconfluence after trypsinization.

Preparation and culture of primary human colon cells
We collected deidentified discarded fresh tissue samples from colon adenocarcinomas and adjacent normal colon from patients undergoing primary colon cancer resection at the University of Maryland Medical Center (Institutional Review Board exemption HP-00085101, 3/20/2019; no organs/tissues were obtained from prisoners).As described previously 64 , after washing (HBSS), we cut tissues into 1-2 mm 3 sections, and placed them in 0.1% trypsin at 4 °C overnight.We then placed tissues in complete growth media (RPMI 1640 supplemented with 10% FBS with an antibiotic-antimycotic) and incubated the material at 37 °C for 15 min.We then washed tissues (HBSS) before additional incubation in 0.1% collagenase for 45 min at 37 °C (5% CO 2 ).After filtration (40-μm filters), we centrifuged cells at 150 × g for 5 min at room temperature, resuspended cells in culture media, and seeded cells in T25 flasks.

Proximity ligation assay (PLA)
We used the Duo-link In Situ-Fluorescence kit following both the manufacturer's instructions (Sigma-Aldrich) and published methods 65 .Briefly, we grew fresh primary cancers on slides, fixed in cold MeOH for 10 min and permeabilized with 0.1% Triton-X-100 for 10 min on ice.We incubated cells with blocking solution for 60 min and incubated overnight (4 °C) with anti-βPix and -β-catenin antibodies.We then incubated cells with PLA probes for 1 h, with ligation solution for 30 min, and amplification solution for 100 min (all at 37 °C).To identify cell nuclei, we stained slides with 4' ,6-diamidino-2-phenylindole (DAPI).We acquired images using an LSM 510 inverted confocal microscope; dots in the cell nucleus represented βPix molecules within 40 nm of β-catenin molecules.

Quantitative RT-PCR (qPCR)
As described previously 59 , we synthesized first-strand cDNAs from 5 µg RNA (Superscript III First Strand Synthesis System for RT-PCR, Invitrogen) and performed qPCR using 50 ng cDNA, the SYBR Green PCR Master Mix (Applied Biosystems), and 0.5 μM in 20 μl forward and reverse primers.We designed primers (Supplemental Table 1) to span introns using the National Center for Biotechnology Information nucleotide database SIM-4 gene alignment program and on-line software (www.gensc ript.com/ ssl-bin/ app/ primer).We performed qPCR using Step One (Applied Biosystems) with Power SYBR Green Master Mix (ABI).PCR conditions were as follows: 5 min at 95 °C followed by 37 cycles of 95 °C for 15 s, 60 °C for 20 s, 72 °C for 40 s, and final cycles at 95 °C for 15 s, 60 °C for 15 s, and 95 °C for 15 s.We normalized gene expression to β 2 -microglobulin (B2M) and analyzed qPCR data using the comparative C T (2 -ΔΔC T ) method.

Immunoblotting and immunoprecipitation
For immunoblotting, we treated cells with MR agonists and antagonists at the concentrations and times indicated and, as described previously 38 , lysed cells in 20 mM Tris, pH 7.5, 100 mM NaCl, 5 mM MgCl 2 , 1 mM EDTA, 1% Triton X-100, 1 mM sodium fluoride, 1 mM sodium vanadate, 1 mM phenylmethylsulfonyl fluoride, 1 µg/ml pepstatin, and 1 µg/ml leupeptin.We separated equal amounts of protein by 7.5% sodium dodecyl sulfate-polyacrylamide gel electrophoresis, transferred onto polyvinylidene difluoride membranes (Millipore), immunoblotted, and visualized bands by chemiluminescence (Amersham Biosciences).For immunoprecipitation, we added antibodies against β-catenin or βPix to cytoplasmic or nuclear lysates for 2 h, followed by protein A-or protein G-agarose beads for 1 h.We washed beads thrice in PBS, released immunoprecipitated proteins from beads by boiling in 1 × sample buffer (5 min), and immunoblotted.We employed β-actin and H2A loading controls to ascertain that equal amounts of cytoplasmic and nuclear proteins, respectively, were included in the extracted protein input.After immunoprecipitation, as a second loading control, we immunoblotted for expression of the bait protein (e.g., βPix following immunoprecipitation with anti-βPix antibody); this is marked by a vertical line to the left of the images obtained from the same gel.

Fluorescence cell sorting
Applying methods described previously 67 , we seeded HT-29 cells (4.5 × 10 6 cells) in 60-mm plates for 24 h.We serum starved cells for 24 h before adding 200 µM ACh for 10 min.After trypsinization, we fixed cells with 1% PFA on ice for 15 min and filtered them through 40-µm filters.We resuspended cells in 80% ethanol, incubated them for 4 min on ice, and washed with PBS.We blocked cells in PBS with 7% donkey serum and 0.1% TX-100 for 30 min at room temperature before adding primary anti-β-Pix and anti-activated β-catenin antibodies for 1 h at 4 °C.After washing with PBS, we incubated cells with secondary antibody (Alexa488; 30 min at 4 °C).
We washed cells with PBS, stained nuclei with DAPI at room temperature (15 min) and washed again with Ca 2+ /Mg 2+ -free DPBS.We performed flow cytometry and measured intracellular fluorescence (ImageStreamX MKII high-speed imaging flow cytometer; Amnis).We collected bright field and fluorescent images (AF488 at 480-560 nm; DAPI at 435-505 nm, and AF555 at 560-595 nm) at a × 60 magnification.To determine nuclear localization of β-Pix (AF488 attached) and activated β-catenin (AF555 attached), we analyzed 5,000 gated cell singlets per sample and used IDEAS Analysis Software (Amnis) and the Similarity Morphology Feature.

Colon cancer cell proliferation, migration, and invasion assays
For cell proliferation assays, we seeded HCT116 cells at 7 × 10 3 cells per well and transfected cells with 50 nM control or βPix siRNA using TransIT-siQuest reagent according to the manufacturer (Mirus).After 24 h, we stimulated cells with 100 µM ACh for 48 h and measured cell proliferation using the CellTiter-Glo assay kit (Promega).For cell migration assays, we placed HT-29 cells in the upper chamber of uncoated inserts (BD Biosciences).Cells on the underside of inserts were fixed, stained (Hema 3; Fisher), and counted in five random high-power fields (HPF).We performed Invasion assays using Biocoat Matrigel Invasion Chambers (Corning) as described previously 6,52 .

Induction of murine colon neoplasia
We treated 10-to 17-week-old Arhgef7 CKO and littermate control male and female mice with once weekly intraperitoneal injection of 7.5 mg AOM/kg body weight for four weeks.Starting one week after the last AOM injection, 2.5% DSS was added to the drinking water for 5 days.In a separate experiment, after AOM/DSS treatment, we added bethanechol (400 µg/ml) to the drinking water for 15 weeks.Twenty weeks after the first AOM injection, investigators masked to genotype euthanized mice, harvested colons, and measured tumor number and size.

Online cancer databases
We used Oncomine™ (www.oncom ine.org) 44 to compare gene mRNA levels in colon cancer and normal adjacent tissue.GEPIA (gepia.cancer-pku.cn)analyzes RNA expression in tumor and normal samples from the National Cancer Institute Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) databases 45 .
The Human Protein Atlas Program provided information on proteins in cells, tissues, and organs 46 and used UALCAN (ualcan.path.uab.edu) to analyze OMICS data 47 .We compared ARHGEF7, CHRM3, and PTSG2 mRNA expression levels as described 57 .

Statistical analysis
Unless indicated otherwise, we expressed data as mean ± SE from at least three experiments and analyzed results using Student's two-tailed t-test, Mann-Whitney U test, one-way ANOVA, with either Tukey's HSD post hoc or Dunn's tests using SigmaPlot 13.0 (Systat Software, Inc., San Jose, CA) and two-tailed Fisher's exact test using GraphPad Prism (San Diego, CA).We considered a p-value < 0.05 statistically significant.

Figure 1 .
Figure 1.Colocalization of β-catenin and βPix in the nuclei of human colon cancer cells that overexpress M 3 R.(a) Overexpression of M 3 R, but not M 1 R, was observed in colon cancer stem cells.Images show H&E (left panels) and immunofluorescent staining with DAPI (nuclear stain, blue), CD133 (red-Alexa Fluor 594), M1R, and M3R (both green-Alexa Fluor 488), and merged images.Dashed boxes in H&Es show areas from which images were enlarged.CD133 staining reveals scattered colon cancer stem cells (white arrow) and colon cancer stem cell clusters around blood vessels (invasive front; yellow arrows).Top panels: M 1 R overexpression was not detected in colon cancer stem cells.Bottom panels: M 3 R overexpression was detected in colon cancer stem cells.Size bars in H&E images are 50 µm for M 1 R staining and 100 µm for M 3 R staining.(b) β-catenin and βPix colocalize in the nucleus of invasive human colon adenocarcinoma cells.Normal colon (top) and poorly differentiated cancer (bottom) tissues obtained at surgery from the same person were stained with H&E and DAPI, and immunostained with anti-β-catenin and anti-βPix antibodies.In normal colon and the cancer core, β-catenin and βPix staining was primarily membranous (arrowheads).In contrast, in cells at the invasive front (delineated by dashed lines in the H&E and merged images), β-catenin and βPix were co-localized to dysplastic nuclei (arrows).Size bars are 20 μm except for 5 μm in the high magnification (High Mag) images.Images are representative of n = 6 cancers.

Figure 3 .
Figure 3. MR activation stimulates βPix binding to β-catenin.(a-f) At the times shown, HT-29 cells were treated with 300 μM ACh.Cytosolic (a, c) and nuclear (b, d) fractions were probed after IP. (e-f) Pre-incubating cells with atropine (Atr, 5 μM for 30 min) for the indicated times blocked ACh effects in both the cytosol (e)and the nucleus (f).Ctl, control; β-actin and histone 2A (H2A) were used as cytosolic and nuclear fraction loading controls.(g) HT-29 and H508 human colon cancer cells were treated with 100 µM carbamylcholine (carb).Nuclear fractions were probed for βPix after IP; histone 2A (H2A) is a loading control.(h) Relative density (au, arbitrary units) was measured in six different βPix immunoblots performed as illustrated in (g), normalized to the loading control, and expressed as a function of βPix expression in unstimulated cells.N = 3 and 6 experiments for HT-29 and H508 cells, respectively.Ctl, control.Histone 2A (H2A) was a nuclear loading control.(i) HT-29 cells were pre-incubated with inhibitors of EGFR (AG1478) and PKCα/β1 (Gö6976) for 60 min before adding 300 µM ACh for an additional 10 min.After treatment, nuclear fractions were immunoprecipitated with anti-βPix antibody followed by immunoblotting as indicated.Histone 2A (H2A) was a nuclear marker.(j) In the left panel, HT-29 cells were treated with 50 nM PMA for 10 min with or without preincubation for 45 min with a PKC inhibitor (5 μM Gö6976).In the right panel, HT-29 cells were incubated with 10 ng/ml EGF for 10 min with or without preincubation for 60 min with EGFR (5 µM PD153035) and MEK (10 µM U0126) inhibitors.Nuclear fractions were probed by immunoprecipitation with anti-βPix antibody and immunoblotting with anti-β-catenin and anti-βPix antibodies.MW, molecular weight.Original uncut immunoblots are shown in Supplemental Materials.

Figure 5 .
Figure 5. βPix deficiency attenuates MR agonist-induced changes in colon cancer cell function.(a) Extracts from control HCT116 cells and cells transfected with siRNA directed against ARHGEF7 or control siRNA were immunoblotted for βPix.βPix expression was reduced by siRNA directed against ARHGEF7 but not altered by transfection with control siRNA.β-actin was a loading control.(b) βPix contributes to MR agonistinduced colon cancer cell proliferation.Control HCT116 cells and cells transfected with 50 nM siRNA directed against ARHGEF7 or 50 nM control siRNA were stimulated with 100 μM ACh for 48 h.Cell proliferation was measured using the CellTiter-Glo assay.Results are means of at least three independent experiments in triplicate.*, p < 0.05.(c) Extracts from control HT-29 cells and HT-29 cells transfected with siRNA directed against ARHGEF7 or control siRNA were immunoblotted for βPix.βPix expression was reduced by ARHGEF7 siRNA but not altered by treatment with 100 μM acetylcholine (ACh) for 24 h or transfection with control siRNA.β-actin was a loading control.(d) βPix knockdown attenuates colon cancer cell migration.HT-29 cells, placed in the upper chamber of uncoated inserts, were stimulated with 100 μM ACh for 24 h.Cells migrating to the underside of inserts were fixed, stained, and counted using light microscopy.Bars represent mean ± SE from three individual experiments.Symbols represent results from individual experiments (n = 3 per condition).(e) Immunoblotting confirms βPix protein expression was reduced by transfecting HT-29 cells with shRNA directed against ARHGEF7.GAPDH was a loading control.(f) βPix knockdown attenuates ACh-induced human colon cancer cell invasion.HT-29 cells were placed in the upper chamber of Matrigel-coated inserts and stimulated with vehicle or 100 μM ACh for 48 h.Cells invading to the underside of inserts were fixed, stained, and counted using light microscopy.(g) βPix knockdown attenuates ACh-induced colon cancer cell invasion.Bars represent mean ± SE from four individual experiments.Symbols represent individual experiments (n = 4 per condition).(h) shRNA knockdown of ARHGEF7 expression reduced PTGS2 mRNA levels p < 0.001).mRNA levels were measured by qPCR and normalized to β-2 macroglobulin.MW, molecular weight.Original uncut immunoblots for (a, c), and e are shown in Supplemental Materials.

Figure 6 .
Figure 6.Colon neoplasia is attenuated in βPix-deficient mice.(a) Treatment scheme for azoxymethane (AOM)/dextran sodium sulfate (DSS)-induced colon neoplasia in mice.Colon neoplasia was induced with four weekly intraperitoneal injections of 7.5 mg AOM/kg mouse body weight.One week after the last dose of AOM, 2.5% DSS was added to the animals' drinking water for five days.In some experiments, bethanechol (400 µg) was added to the animals' drinking water for 15 weeks after AOM/DSS treatment.Mice were euthanized 20 weeks after the first AOM injection and their colons were harvested for analysis.(b) Mouse body weights over the 20-week treatment period.Arhgef7 CKO and littermate control mouse weights were similar, including an approximately four-week period of weight loss associated with DSS treatment.Regardless of genotype, female mice weighed approximately 20% less than male mice.(c) Colon tumor numbers were reduced in Arhgef7 CKO mice.CKO mice (n = 30) had fewer colon tumors than control mice (n = 32) (p = 0.04).Each symbol represents the number of colon tumors detected in one mouse.Bars represent means ± SE.(d) Reduced numbers of adenocarcinomas in AOM/DSS-treated Arhgef7 CKO mice.Bar graph shows 24% fewer adenomas and 55% fewer adenocarcinomas in CKO compared to control mice.(p = 0.04).(e) Colon tumor numbers were reduced in Arhgef7 CKO mice treated with a MR agonist.After AOM/DSS treatment, bethanechol (400 µg/ ml) was added to the animals' drinking water for 15 weeks.CKO mice (n = 18) had substantially fewer colon tumors than littermate control mice (n = 20) (p = 0.03).Each symbol represents the number of colon tumors detected in one mouse.Bars represent means ± SE. (f) Expression of colon cancer-related genes was measured in adenocarcinomas harvested from 10 AOM/DSS-treated Arhgef7 CKO and 14 littermate control mice.Each symbol represents the mRNA level in an adenocarcinoma from one mouse relative to the mean values for that gene in control mice (arbitrarily set at 1).Bars represent means ± SE.(g) Representative immunoblots show paired expression of colon cancer-related proteins in normal colon and colon adenocarcinomas harvested from AOM/DSS-treated littermate control (n = 6) and Arhgef7 CKO (n = 6) mice.Original uncut immunoblots are shown in Supplemental Materials.