The gastrin and cholecystokinin receptors mediated signaling network: a scaffold for data analysis and new hypotheses on regulatory mechanisms
© Tripathi et al. 2015
Received: 9 March 2013
Accepted: 16 June 2015
Published: 24 July 2015
The gastrointestinal peptide hormones cholecystokinin and gastrin exert their biological functions via cholecystokinin receptors CCK1R and CCK2R respectively. Gastrin, a central regulator of gastric acid secretion, is involved in growth and differentiation of gastric and colonic mucosa, and there is evidence that it is pro-carcinogenic. Cholecystokinin is implicated in digestion, appetite control and body weight regulation, and may play a role in several digestive disorders.
We performed a detailed analysis of the literature reporting experimental evidence on signaling pathways triggered by CCK1R and CCK2R, in order to create a comprehensive map of gastrin and cholecystokinin-mediated intracellular signaling cascades. The resulting signaling map captures 413 reactions involving 530 molecular species, and incorporates the currently available knowledge into one integrated signaling network. The decomposition of the signaling map into sub-networks revealed 18 modules that represent higher-level structures of the signaling map. These modules allow a more compact mapping of intracellular signaling reactions to known cell behavioral outcomes such as proliferation, migration and apoptosis. The integration of large-scale protein-protein interaction data to this literature-based signaling map in combination with topological analyses allowed us to identify 70 proteins able to increase the compactness of the map. These proteins represent experimentally testable hypotheses for gaining new knowledge on gastrin- and cholecystokinin receptor signaling. The CCKR map is freely available both in a downloadable, machine-readable SBML-compatible format and as a web resource through PAYAO (http://sblab.celldesigner.org:18080/Payao11/bin/).
We have demonstrated how a literature-based CCKR signaling map together with its protein interaction extensions can be analyzed to generate new hypotheses on molecular mechanisms involved in gastrin- and cholecystokinin-mediated regulation of cellular processes.
Gastrin and cholecystokinin (CCK) are gastrointestinal peptide hormones that share a common C-terminal pentapeptide amide . Gastrin, produced in G-cells of the gastric antrum, is the central regulator of gastric acid secretion but also regulates growth and differentiation of gastric and colonic mucosa . CCK, produced primarily in I-cells of the small intestine, is involved in physiological processes such as digestion, appetite control and body weight regulation . The scientific interest in these hormones is further strengthened by their roles in several diseases. Indeed, CCK has been implicated in acute pancreatitis [4–6], obesity [7, 8], irritable bowel syndrome  and gall bladder disease [10, 11]. Gastrin is known to be pro-carcinogenic, affecting proliferation, angiogenesis and apoptosis , and is a risk co-factor for gastric carcinogenesis and atrophy upon Helicobacter pylori infection [12, 13]. In order to efficiently study and understand the molecular mechanisms triggered by gastrin and cholecystokinin, detailed knowledge concerning the signaling pathways they regulate is paramount.
Information concerning intracellular signaling is commonly retrieved from databases such as Reactome  and KEGG . However, none of these resources currently specify which specific molecular events are known to take place in response to gastrin or CCK. Researchers in need of such knowledge therefore must spend significant time reviewing current literature in order to gain an exhaustive and up-to-date understanding of the signaling network. A comprehensive map of gastrin and CCK intracellular signaling pathways would significantly assist in the study of normal or aberrant cholecystokinin receptor (CCKR) signaling.
In the past decade, several manually constructed maps of signaling events have been published [16–25], each providing solid foundations for a systems understanding of the signaling mechanisms. The present work extends this approach to the domain of CCKR signaling by providing a comprehensive literature-based CCKR signaling map that comprises 530 molecular species and 431 reactions, considerably extending previously compiled knowledge on CCK2R signaling [10, 26] including CCK1R downstream events.
Partitioning the total CCKR signaling map into sub-networks using the BiNoM tool  resulted in 18 modules that coordinate with each other to elicit the diverse intracellular signaling responses to gastrin and/or CCK. Finally, we used the CCKR map as a scaffold for protein-protein interaction (PPI) data integration assisted by PathExpand , in order to predict novel components of the signaling network. This resulted in the identification of 70 new proteins tightly connected to the CCKR signaling map, making them prime candidates for future experimental work aimed at further extending knowledge on regulation of CCKR mediated signaling mechanisms.
Construction of the CCKR map from literature
- i).Knowledge encoded in the CCKR map was obtained from scientific publications that were identified by searching for different combinations of cholecystokinin (CCK)/CCK1R and gastrin (G-17)/CCK2R in PubMed or through various literature mining tools, e.g. LitInspector (http://www.genomatix.de/solutions/genomatix-software-suite.html)  and iHOP (http://www.ihop-net.org/UniPub/iHOP/) . We adopted two main criteria as guidelines for including a scientific paper for the information extraction, namely that it must contain:
evidence that the reported signaling event is mediated by the specific interaction of CCK or gastrin (G-17) with their receptors CCK1R and CCK2R.
signaling information to allow for linkage of a new CCKR map component to its upstream and/or downstream regulators in CCKR signaling.
CellDesigner species and reaction “note” features were used to record PubMed IDs (PMID), cell-type specific information for each reaction, and the interacting components in the CCKR map.
- iii).Final curation and quality control was done in a collaborative effort involving five different research group members who collectively used the community curation platform PAYAO (http://www.payaologue.org) , enabling efficient exchange of comments and tags. Consensus and critical comments from each annotator about the precise representation of reactions, components, and their cellular localization were discussed and implemented (Fig. 1). Finally, the CCKR map was published with an open source license for the whole scientific community through PAYAO  (map available at: http://sblab.celldesigner.org:18080/Payao11/bin/). The CCKR map is also available in the SBML data exchange format (Additional file 1), and we are also in the process of submitting this map to the PANTHER database .
We welcome comments and tags from a community of curators to continue increasing the quality of this CCKR signaling map and will keep it up to date with our growing biological understanding.
Analysis of the CCKR map
Network topology studies were performed by importing the CellDesigner-generated SBML file of the CCKR map to Cytoscape version 2.8  using the BiNoM plugin , after removing connections downstream of the transcription factor layer. BiNoM considers both ‘reaction’ and ‘species’ of a CellDesigner map as a node. The Cytoscape version of the CCKR map consisted of 807 nodes (475 species and 332 reactions) with 963 edges. Node degree and closeness centrality were calculated using the ‘Network Analysis’ plugin  in Cytoscape, assuming the network to be undirected. The number of nodes connected directly to a particular node defines its node degree k, and the node degrees of all nodes in the network represent the ‘degree distribution’ of the network. Nodes with degree k > 5 were termed ‘hubs’.
BiNoM decomposition of CCKR map into modules
We used the ‘prune the graph’ function of BiNoM to automatically separate the strongly connected component (SCC), i.e. the central cyclic motif of the map, from more loosely connected upstream and downstream species. The SCC was further decomposed into smallest sub-networks with the function ‘extract material components’. Next, some manual curation work was performed: sub-networks with 50 % or more overlapping nodes were clustered together while the large sub-networks were decomposed further until each sub-network contained a unique central cyclic motif. Any unconnected nodes were removed from the sub-networks, yielding a total of 18 sub-networks or modules. Next, these 18 modules were merged together and the resulting network was compared with the initial map to check for completeness in terms of any missing interactions or nodes. The complete map and its 18 decomposed modules are available as a Cytoscape session file (Additional file 2).
Protein-protein interaction based expansion of the CCKR map
PPI data were downloaded using PSICQUIC (all databases, version June 2012), and filtered for binary physical interactions based on PSI-MI controlled vocabulary experimental method descriptions, following the procedure in  (Charles E. Chapple, personal communication). We then tested each of the 4119 proteins found to interact with CCKR signaling map proteins with the PathExpand method  to seek for tightly linked protein interactors that enhance the network compactness of the CCKR map by leading to higher node degree, betweenness and average local clustering as well as decreasing the shortest path lengths (for details see ) .
CCK and gastrin impinge on cellular functioning by binding to two different G protein-coupled receptors, CCK1R and CCK2R, respectively, located at the surface of multiple cell types in peripheral organs such as the gastrointestinal tract, the pancreas, and the gall bladder . Today, no comprehensive resource exists that compiles current knowledge on CCKR activated signaling pathways. Gastrin has a strong preference for CCK2R, while CCK can activate both receptors with similar affinities . Most cell types responsive to one or both peptide hormones express only one CCK-receptor variant. However, a range of normal and cancer cells in whole organisms as well as model cell lines (for instance the rat pancreatic acinar cell derived cell-line AR42J ) express both CCK1R and CCK2R.
The CCKR signaling map
Overview of the CCKR map
314 (199 unique)
Heterodimer associations and dissociations
63 (35 unique)
Transcriptions and translations
Figure 2a displays a detailed view of the map depicting the two ligands gastrin and CCK, their biogenesis and processing, their binding to the two G protein coupled receptors CCK1R and CCK2R and the ensuing signal transduction pathways including activation of transcription factors and downstream target genes reported to be triggered in response to gastrin and/or CCK. Moreover, a number of cellular processes influenced by specific CCKR signaling events are indicated, including proliferation, migration, differentiation, anti-apoptosis and inflammation. Figure 2b is an aid for the reader to navigate in Fig. 2a, as it indicates the position of major pathways involved, including protein kinase C (PKC)-dependent activation of MAPK cascades, PI3K-mTOR signaling, protein kinase A (PKA)-dependent pathway, β-catenin, and Rho-GTPase-Bcl cascades.
Signaling pathways shared by CCK1R and CCK2R
Downstream signaling mechanisms shared by CCK1R and CCK2R include the trimeric guanine nucleotide binding alpha q protein (G-protein αq), PKC dependent phosphorylation of adaptor protein SHC - transforming protein C, and its association with GRB2/SOS1 leading to activation of the HRAS/RAF/MAPK1/3 cascade [10, 41, 42]. Other shared pathways involve MAP3K11-mediated regulation of MAPK8, −9 and −10 and p38MAPK (MAPK14), PRKD1 (in PKC signaling), PI3K, AKT1, FAK1, JAK2-STAT3 and Rho GTPase [10, 41–44]. Both receptors activate PKC isoforms PKCα, −δ, −ε, −θ and −ζ [10, 45–47]. Transcription factors reported downstream of both CCK1R and CCK2R receptors include NFκB, CREB1, ELK1 and AP1.
CCK1R-specific signaling pathways
Two trimeric G-proteins appear to be regulated only by CCK1R. One is G alpha S (Gαs) , which leads to Protein kinase A activation via adenylate cyclase catalyzed cAMP production, and the other is G alpha 13 (Gα13) , involved in downstream activation of RHOA . The NOS1 signal transduction pathway downstream of CCK1R [50, 51] regulates Ca2+ signaling pathways by opening ryanodine receptors and two-pore channels that release calcium from the endoplasmic reticulum and endolysosomes, respectively [52–54]. Other signaling cascades, so far only reported for CCK1R, include the Ca2+/calmodulin (CaM) dependent activation of CaMKIV and calcineurin (CaN) – NFAT1 signaling pathways [55–57].
CCK2R-specific signaling pathways
CCK2R activates EGFR via PKC activated MMP3, which cleaves membrane-attached pro-HBEGF into mature HBEGF [58, 59]. PKC isoforms PKC-β and PKC-η have been reported only downstream of CCK2R signaling [60, 61]. CCKR2 specific activation of β-catenin and E-cadherin is mediated by PAK1 [62, 63], and CCK2R specific modulation of BCL-protein family signaling regulates mitochondrial cytochrome C release [64, 65]. CCK2R, but not CCK1R, is reported to activate MAPK7 , an upstream regulator of transcription factors MEF-B,-C and D, and the PKC-η target PRKD2 , which enhances nuclear export of HDAC7 thereby relieving transcriptional repression of target genes such as NR4A1 .
Segmentation of the CCKR signaling map into modules
Overview of the 18 modules and the numbers of defining (specific) components in each module
# defining components
Gastrin-regulated cellular processes involve different sets of signaling modules
Depending on cell type and the state of cells, gastrin can induce different cellular outcomes, such as proliferation, migration and apoptosis. In order to investigate what is known about the involvement of each of the signaling pathway modules in these processes, we checked the scientific literature that we have used to build the CCKR map. We chose to focus on gastrin-mediated effects, because molecular mechanism studies of gastrin-regulated cellular responses are more abundantly reported in literature. Specifically, we recorded all instances where experimental evidence was reported indicating that the function of a specific signaling component had an effect on the cellular outcome in response to gastrin treatment. Based on this literature survey, involvement in cellular outcomes was indicated in Fig. 4a. While central modules such as PKC, AKT1, Rho GTPase, MAP3K11, MAPK1/3 and AP1 are reportedly involved in all three cellular outcomes, other signaling mechanisms are more specific in their effect, e.g. the BCL-module signaling is only observed to be involved in apoptosis (Fig. 4a). Below, we provide a brief description of signaling modules and components involved in each of the cellular outcomes to gastrin treatment.
Molecular mechanisms underlying gastrin-mediated proliferation involve regulation of protein synthesis and cell cycle. Protein synthesis is stimulated via the AKT1-module component mTOR triggering p70 S6 kinase [69, 70]. Gastrin-induced transcription of Cyclin D1, a central regulator of cell cycle progression, is mediated by JUN, FOS, CREB1, and TCF7L2 [71–75], which are components of the modules: AP1, ATF2 and β-catenin. The modular representation (Fig. 4a) shows that EGFR-associated signaling enhances gastrin-induced proliferation by feed-forward mechanisms involving SRC module components. The modular map (Fig. 4a) shows that the AKT1 module inhibits RAF1 and consequently MAPK1/3-module pathways. The molecular mechanism for this is AKT1 kinase-mediated phosphorylation of RAF1 . The modular map thus allows us to hypothesize that the activating role of AP1- and ATF2-submodule signaling in proliferation is more likely to proceed via SRC-MAP3K11 pathways, since these are not inhibited by AKT1.
Gastrin promotes cell migration by activating transcription of MMP7 and MMP9 [77, 78] via transcription factors SNAI1, β-catenin and JUN  represented in the β-catenin- (SNAI1, β-catenin)- and AP1-(JUN) modules. Cell adhesion, tightly linked to cell migration, is regulated through components in the FAK1/2 module (FAK1 and FAK2; Paxillin, CAS, and CRK [79, 80]), which is controlled via both PKC and SRC-modules. The module representation (Fig. 4a) indicates that PKC- and SRC-modules exert a positive feedback regulation on the FAK1/2 module.
Apoptosis is inhibited by gastrin via several mechanisms including BCL-mediated repression of pro-apoptotic caspases and AP1-activated expression of Clusterin [64, 65, 81, 82]. The modular representation reveals that these cellular responses are regulated both by PKC independent and PKC dependent mechanisms. This applies to NFκB and its downstream anti-apoptotic BIRC2 and BIRC3 target genes, which can be activated either directly by PKC or independently of PKC through the Rho GTPase module. Likewise, the AKT1-involvement in regulation of the BCL-module can be mediated by PKC-dependent mechanisms or independently of PKC by the CCK2R - Rho GTPase pathway. Activation of AP1, on the other hand, seems to be strictly dependent on PKC that mediates its effect via either RAF1-MAPK1/3 or SRC-MAP3K11 cascades.
We note that the AKT1-module both inhibits the RAF1-MAPK1/3-route to AP1-activation and enhances Rho GTPase activation of the BCL-module. Thus, AKT1 can potentially promote BCL-module apoptosis-regulating mechanisms and at the same time block MAPK1/3-mediated AP1-activation. In the latter configuration the cell would rely on MAP3K11 to bypass the inhibitory effect of AKT1 on AP1-mediated regulation of gene expression.
Extending the CCKR map with PPI data
The comprehensive CCKR signaling map (Fig. 2) has been constructed with a knowledge-driven approach based on molecular reactions and interactions that are well-documented by scientific evidence in the literature. This thereby inevitably leaves significant gaps concerning signaling events and mechanisms that have not yet been studied and evidenced. We have therefore exploited large-scale PPI data to assess how it can complement the CCKR signaling map by a data-driven strategy.
List of PathExpand interactors
CCK model protein interactors
Annotated in pathway databasesa
actin filament associated protein 1
A kinase (PRKA) anchor protein 14
Rho GTPase activating protein 31
Rho guanine nucleotide exchange factor (GEF) 25
additional sex combs like 1 (Drosophila)
ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6
biliverdin reductase A
BCL2/adenovirus E1B 19 kDa interacting protein 1
coiled-coil domain containing 88A
CD59 molecule, complement regulatory protein
carbamoyl-phosphate synthase 1, mitochondrial
discoidin domain receptor tyrosine kinase 2
dual specificity phosphatase 2
dual specificity phosphatase 22
dual specificity phosphatase 4
dual specificity phosphatase 5
dual specificity phosphatase 7
dual specificity phosphatase 9
eukaryotic translation initiation factor 4E binding protein 2
eukaryotic translation initiation factor 4E binding protein 3
ERBB receptor feedback inhibitor 1
family with sequence similarity 59, member A
Fc fragment of IgG, low affinity IIc, receptor for (CD32) (gene/pseudogene)
FK506 binding protein 1A, 12 kDa
fms-related tyrosine kinase 4
GRB2-associated binding protein 3
gap junction protein, beta 1, 32 kDa
glioma tumor suppressor candidate region gene 1
guanine nucleotide binding protein (G protein), beta polypeptide 1-like
guanylate cyclase 1, soluble, alpha 3
isoprenylcysteine carboxyl methyltransferase
IQ motif containing GTPase activating protein 2
interferon regulatory factor 5
inositol-trisphosphate 3-kinase A
kinase suppressor of ras 1
mitogen-activated protein kinase 15
MCF.2 cell line derived transforming sequence-like
mucin 12, cell surface associated
neutrophil cytosolic factor 1B pseudogene
nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 3
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta
par-6 partitioning defective 6 homolog gamma (C. elegans)
programmed cell death 11
phosphodiesterase 3B, cGMP-inhibited
phosphatidylethanolamine-binding protein 4
PH domain and leucine rich repeat protein phosphatase 1
phosphatidylinositol 4-kinase type 2 beta
phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 beta
pleckstrin homology domain containing, family G (with RhoGef domain) member 2
protein phosphatase 1, regulatory (inhibitor) subunit 14A
protein tyrosine phosphatase, non-receptor type 7
protein tyrosine phosphatase, receptor type, R
RAS guanyl releasing protein 3 (calcium and DAG-regulated)
receptor-interacting serine-threonine kinase 4
ribosomal protein L27
ribosomal protein S6 kinase, 90 kDa, polypeptide 4
SH2 domain containing 3C
signaling threshold regulating transmembrane adaptor 1
TBC1 domain family, member 3 F
TGFB1-induced anti-apoptotic factor 1
transition protein 1 (during histone to protamine replacement)
TPX2, microtubule-associated, homolog (Xenopus laevis)
Inspection of the expanded networks resulting from the combination of PathExpand protein interactors with 7 CCKR modules (Fig. 4b, transcription factor centered modules excluded) shows that 11 of the protein interactors are linked to more than one CCKR module and can contribute both to PKC-independent (e.g. ARHGEF25, ARHGAP31, TBC1D3F) and PKC dependent (e.g. ICMT) signaling routes. In contrast, 21 protein interactors are linked to only one module, suggesting that they may act as preferential regulators of this module. For instance, the Mitogen activated kinase 15 (MAPK15) is a compactness increasing protein only for the SRC module, where it interacts with the two kinases SRC and CSK.
CCKR map and genome-scale PPI generate hypotheses for refinement of Rho GTPase module mechanisms
By taking a closer look at the gastrin regulated Rho GTPase module and its identified PPI extensions, we here discuss putative novel signaling mechanisms involved in gastrin-mediated regulation of the Rho GTPase signaling.
Central to the Rho GTPase module (Fig. 5a) is the activation of small GTPases, RHOA, RAC1, and CDC42 by guanine exchange factor proteins (GEFs), which trigger conversion of the inactive GDP-bound form of small GTPases to the active GTP-bound form. The GEFs in gastrin-mediated Rho GTPase signaling are Leukemia-associated Rho guanine-nucleotide exchange factor (LARG) and the trimeric receptor-associated G-protein complexes Gαq and Gα13. In addition, HRAS may also act to activate RHOA and CDC42. The small GTPases RHOA, RAC1, and CDC42 are documented to activate kinases ROCK1 and PAK1, which are both part of the gastrin-regulated Rho GTPase module, and of kinase AKT1, part of the gastrin-regulated AKT1 signaling module. The inactive form of the small GTPases is restored by GTPase-activating proteins (GAPs) that enhance hydrolyzation of the bound GTP. In gastrin-mediated signaling deactivation of RHOA and RAC1 is effectuated by GAPs, ARHGAP4 and RGS2, respectively.
Eight of the ten PathExpand protein interactors (Fig. 5b, Additional file 5) of Rho GTPase module components interact with one or more of the small GTPases RHOA, RAC1, and CDC42. All of these protein interactors are annotated with GO-terms indicating a known role in regulation of small GTPases, and four of them (IQGAP2, TBC1D3F, ARHGAP31, OPHN1) are known as GTPase activators. We suggest that these eight proteins are strong candidates for potentially novel modulators of gastrin-mediated Rho GTPase module signaling. Three of the proteins (TBC1D3F, ARHGAP25, and ICMT) are not yet present in any of the common pathway databases (see Table 3). The evidence presented here, indicating that the three proteins have tight interaction with multiple proteins involved in gastrin signaling, demonstrates that our approach is well suited to identify testable hypotheses, even for candidates for which knowledge in public databases is still sparse.
The PathExpand interactor BNIP1 (BCL2/adenovirus E1B 19 kDa interacting protein 1) interacts with two downstream BCL module components BCL2L1 and BCL2, both involved in effectuating the gastrin anti-apoptotic signal. Since BNIP1 is known to be involved in SNARE vesicular transport, our findings indicate that it may be an interesting candidate to follow up with investigating a potential role of vesicular transport in modulating BCL-linked signaling mechanisms in the gastrin signaling pathway. The PathExpand interactor programmed cell death 11 (PDCD11) interacting with the two subunits of NFκB transcription factor (NFκB1 and TF65) is known to be involved in maturation of ribosomal RNA but may also play a role in mRNA processing. Our results identify PDCD11 as a potential candidate to follow up in experimental analysis of molecular mechanisms involved in NFKB-mediated gene regulation in cellular responses to gastrin.
In the work presented here, we set out to build a comprehensive and well-annotated molecular interaction map to aid future studies involving gastrin or CCK. A mechanistic understanding of CCK1R and CCK2R signaling networks is essential for experiment design and data interpretation in biological systems involving gastrin- and CCK-regulated processes. Moreover, it may enhance the identification of therapeutic chemicals able to target disease, by using the map as a functional interaction diagram with components that modeling indicates as prime targets for perturbation, as described by Lee et al. , who successful designed a drug-induced rewiring of the ‘state’ of oncogenic signaling networks to maximize the susceptibility to anticancer drugs. The current map depicting molecular signaling mechanisms underlying CCK1R and CCK2R triggered cellular responses may provide a tool to guide further investigations into normo- and pathophysiological processes such as gastrin-regulated stomach mucosa homeostatis and gastrin-linked carcinogenesis [59, 64, 85, 86], and cholecystokinin-induced hypoplasia, cell regeneration and digestive enzyme secretion  as well as to identify potential intervention strategies for associated disease states.
Some pathway proteins and reactions of the CCKR signaling map are also described in the Reactome  and KEGG  databases. However, the CCKR map constitutes a vastly more comprehensive and integrated model, providing detailed signaling reactions linking the receptors CCK1R and CCK2R all the way to regulated genes and cellular responses. For comparison, the recently published gastrin signaling map  comprises approximately half of the molecules and only a quarter of the reactions presented in our CCKR map. Similarly, knowledge currently in Reactome covers less than 5 % of the pathway details presented here. The CCKR map therefore represents a significant increase in curated signaling information. The provided SBML version of the CCKR map can serve as a starting point to generate quantitative mathematical models  for simulation and prediction of cellular outcomes in response to perturbations of the network.
We enhance the applicability of the map for hypothesis generation by two central strategies. First, we provide a computationally modularized version of topologically and functionally connected meta-nodes. This modular view simplifies the complete CCKR map and provides for an improved, higher level comprehension of pathway regulatory aspects concerning cell fate decisions related to proliferation, migration and apoptosis. Secondly, we take advantage of public large scale PPI knowledge to predict new potential regulators of CCKR signaling, including 70 interactors that significantly enhance the compactness of the CCKR map , through tight direct and indirect interactions with map proteins. Although experimental validations are needed to confirm these new CCKR signaling mechanisms, they represent an important source of high quality hypotheses that may be taken as a first step to develop a better comprehension of CCKR pathway functionality.
Compared to other recently published computational approaches for high-throughput hypothesis generation [20, 89, 90], the advantage of our strategy is the combination of i) biological background knowledge encoded in the signaling map, including the modules, manually curated from literature reporting detailed experimental analyses of gastrin- and CCK-signaling, and ii) large-scale PPI information downloaded from available databases of interactions, filtered for binary physical interaction based on selected experimental detection methods.
Our work demonstrates how publicly available tools can aid in the manual curation of an extensive network topology, in order to build a foundation for a systems understanding of CCKR-mediated cellular responses. Furthermore, the integration of a comprehensive model of complex biological networks with genome scale data can provide new knowledge and hypotheses on molecular mechanisms underlying cellular processes. Further development of the resources presented here should be of high interest in translational research aimed at identifying new targets and biomarkers for treatment and diagnostics of gastrin- and/or cholecystokinin-related disease, including cancer.
We thank Charles E. Chapple for sharing his protein-protein interaction network and Enrico Glaab for “a la carte” PathExpand analyses. This work was supported by The Norwegian Cancer Society, The Liaison Committee between the Central Norway Regional Health Authority (RHA), the Norwegian University of Science and Technology (NTNU) and Sør-Trøndelag University College (HiST).
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