MIF/CD74 axis is a target for novel therapies in colon carcinomatosis
- Fabio Bozzi†1,
- Angela Mogavero†2, 3,
- Luca Varinelli†4,
- Antonino Belfiore1,
- Giacomo Manenti5,
- Claudio Caccia6,
- Chiara C. Volpi1,
- Galina V. Beznoussenko7,
- Massimo Milione1,
- Valerio Leoni6,
- Annunziata Gloghini1,
- Alexandre A. Mironov7,
- Ermanno Leo8,
- Silvana Pilotti1,
- Marco A. Pierotti3,
- Italia Bongarzone4Email author and
- Manuela Gariboldi2, 3
© The Author(s). 2017
Received: 17 September 2016
Accepted: 13 December 2016
Published: 23 January 2017
Strategies aimed at obtaining a complete cytoreduction are needed to improve long-term survival for patients with colorectal cancer peritoneal carcinomatosis (CRC-pc).
We established organoid models from peritoneal metastases of two naïve CRC patients. A standard paraffin inclusion was conducted to compare their 3D structure and immunohistochemical profile with that of the corresponding surgical samples. RNA expression levels of the CRC stem cell marker LGR5 was measured by in situ hybridization. The secretome of organoids was profiled by mass spectrometry. Energy homeostasis of organoids was interfered with 4-IPP and metformin. Biochemical and metabolic changes after drug treatments were investigated by western blot and mass spectrometry. Mitochondria impairment was evaluated by electron microscopy and mitotraker staining.
The two organoids recapitulated their corresponding clinical samples in terms of 3D structure and immmunoistochemical profile and were positive for the cancer stem cells marker LGR5. Proteomic analyses of organoids highlighted their strong dependence on energy producing pathways, which suggest that their targeting could be an effective therapeutic approach.
To test this hypothesis, we treated organoids with two drugs that target metabolism acting on AMP-activated protein kinase (AMPK), the main regulator of cellular energy homeostasis, which may act as metabolic tumour suppressor in CRC. Organoids were treated with 4-IPP, an inhibitor of MIF/CD74 signalling axis which activates AMPK function, or metformin that inhibits mitochondrial respiratory chain complex I.
As a new finding we observed that treatment with 4-IPP downregulated AMPK signalling activity, reduced AKT phosphorylation and activated a JNK-mediated stress-signalling response, thus generating mitochondrial impairment and cell death. Metformin treatment enhanced AMPK activation, decreasing the activity of the anabolic factors ribosomal protein S6 and p4EBP-1 and inducing mitochondrial depolarization.
We provide evidence that the modulation of AMPK activity may be a strategy for targeting metabolism of CRC-pc organoids.
KeywordsOrganoids Metabolism AMPK 4-IPP Macrophage migration inhibitory factor Metformin
Intraperitoneal dissemination is a common progression feature for colorectal cancer (CRC). For the past two decades, aggressive treatments of CRC peritoneal carcinomatosis (CRC-pc), such as cytoreductive surgery plus hyperthermic intraperitoneal chemotherapy, has improved long-term survival . However, the majority of cases present widespread metastases which cannot be destroyed by systemic chemotherapy; therefore, the development of new strategies to prevent the progression of metastatic disease is imperative.
Tumour-initiating, or cancer stem cells (CSCs), have a key role in metastatic CRC (hepatic and/or lung) and chemotherapy resistance ; however, limited information is known about the role of CSCs in CRC-pc development. The first step towards the identification of new therapeutic alternatives requires the development of dedicated pre-clinical models that in vitro and in vivo recapitulate the biological features of CRC-pc.
Past years have seen unprecedented developments of three-dimensional (3D) cultures called cancer organoids. A CRC organoid is obtained by allowing cells (derived from a primary tumour specimen) to self-organize into a 3D structure that recapitulates the original glandular organization commonly observed in human CRC surgical samples. Organoids grow as irregular compact structures, and can be expanded indefinitely and represent the physiology of native tumours much better than traditional cell lines . We have established (in serum-free medium) two CRC-pc organoid cultures of peritoneal metastatic lesions from two CRC patients that showed enrichment in the expression of the CRC CSC marker leucine-rich repeat containing G protein-coupled receptor 5 (LGR5) a member of the canonical WNT pathway and a well-recognized marker of the cell progenitor population located at the crypt-base [4, 5].
In this study, we hypothesized that CRC organoids may secrete a variety of growth factors, cytokines, proangiogenic factors, exosomes, and even extracellular matrix components, some of which are fundamental for maintaining self-renewal and proliferative capacity. Using the advantageous properties of “serum-free” growth conditions for both organoids, we searched for factors with potential therapeutic relevance in their “secretome” compartment produced during cell culture . We found the prominent expression of metabolic pathways mainly related to oxidative homeostasis and glucose metabolism and focused on the macrophage migration inhibitory factor (MIF)/CD74/mitochondria axis, and on the relative 4-iodo-6-phenylpyrimidine (4-IPP) inhibitor, as playing an important role in JNK modulation of the cellular response to reactive oxygen species . To further examine the importance of targeting metabolism in organoids, we studied the effects of direct perturbation of mitochondrial integrity using metformin, which inhibits respiratory-chain complex I, thus inducing a pro-cell death decline in energy status.
Cell culture and tissue samples
Two cancer organoids (CRC-pc1 and CRC-pc2, hereinafter referred to as C1 and C2) were established from peritoneal metastases of naïve patients with stage IV, grade 2 (C1) and grade 3 (C2) CRC following protocols and conditions published by Sato T et al. . BRAF and KRAS mutation patterns in organoids reflected those in the original tumours. Formalin fixed paraffin embedded (FFPE) tissue samples obtained from additional CRC-pc patients (C3, C4 and C5) were included in the study for validation experiments.
The two organoids were maintained in F-12 medium (DMEM F12, Gibco, Carlsbad, CA, USA) as previously described .
This study was approved by the Institutional Review Board of Fondazione IRCCS Istituto Nazionale dei Tumori and each patient provided written informed consent to donate remaining tissues after diagnostic procedures.
Morphology and immunohistochemistry
A standard paraffin inclusion of both organoids was conducted to compare their 3D structure and immunohistochemical profile with those of the corresponding surgical samples. Immunohistochemistry was done with 3-μm FFPE tissue sections. The antibodies used for immunohistochemistry analyses are listed in Additional file 1: Table S1.
In Situ Hybridization (ISH)
ISH for LGR5 RNA expression was manually performed using the RNAscope 2.0 High Definition detection kit (Brown) (Advanced Cell Diagnostics, Inc., Hayward, CA) assay according to the manufacturer’s instructions. Briefly, 5 μm FFPE tissue sections were incubated with Pretreat buffers 1, 2 and with Pretreat Buffer 3 at 40 °C. Slides were hybridized with probes of interest for 2 h at 40 °C, followed by incubations with amplifier reagents 1–6, color development with 3, 3′- diaminobenzine (DAB) and counterstaining with haemotoxylin. RNAscope probes used were LGR5 (311021), the negative control bacterial DapB (310043) and endogenous UBC (310041), used as positive control. Positive staining signals were identified as brown punctuate dots present in the cytoplasm and/or nucleus .
Nano-scale liquid chromatographic tandem mass spectrometry (nLC-MS/MS) analysis
Proteins secreted in the medium (secretome) by C2 organoids were collected and the secretome was profiled as previously described .
Statistical and GO (Gene Ontology) analyses
The Search Tool for the Retrieval of INteracting Genes/proteins (STRING) database  (9.1 version (Database issue):D412-416) was used for prediction of protein subcellular localization. Resulting proteins were also analysed using PANTHER (Protein ANalysis THrough Evolutionary Relationships) system (http://www.pantherdb.org) . Network analyses were performed using the Ingenuity Pathways Analysis (Ingenuity Systems) software.
Sample preparation, SDS-PAGE and immunoblotting
Organoids were cultured for 18 h, and exposed to drugs for the times indicated. Cell pellets were solubilized as previously described . Protein concentrations, SDS-PAGE and electroblotting were determined and performed as previously described . The antibodies used for western blotting analyses are listed in Additional file 1: Table S2.
Trypan blue exclusion
A standard trypan blue exclusion assay was used to evaluate cell viability after 4-IPP and metformin treatments. Data were analyzed using Student’s t-test.
For cell treatments, 88.5 mM of 4-iodo-6-phenylpyrimidine (4-IPP) (Calbiochem, Milan, Italy) and 1 M metformin (Sigma-Aldrich, St. Louis, MO, USA) in 100% DMSO and in PBS 1×, respectively, were diluted directly in the cell culture medium to achieve the working concentrations. The final solvent and vehicle concentrations were less than 0.1% for all samples, including controls.
Isotope dilution mass spectrometry analysis
C2 organoids were treated with 50 or 100 μM 4-IPP and 5 mM metformin. After 24 h, treated cells were lysed and the lysates were analysed by isotope dilution mass spectrometry, as previously described .
Reactive oxygen species detection
C2 organoids were seeded into a 96-well plate. After 24 h, cells were treated with 5 mM metformin for 120 h and with 100 μM 4-IPP for 6 h. Extracellular H2O2 formation was detected and quantified using the ROS-Glo H2O2 assay (Promega, Madison, WI, USA) according to instructions provided by the manufacturer. Luminescence intensity was quantified using a microplate reader (Infinite 200, TECAN Group, Ltd., Männedorf, Switzerland).
Mitochondrial membrane potential analysis
Mitochondrial membrane potential of cells was detected using a MitoProbe™ JC-1 Assay Kit for flow cytometry (Thermo Fisher Scientific Corporation, Carlsbad, CA, USA) after treatment with drugs for the times indicated. Flow cytometry analyses were performed as previously described .
Cells were fixed by addition of 2.5% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.2) for 2 h . Next, samples were post-fixed with reduced OsO4 for 1 h . Osmium staining was treated with 0.3% thiocarbohydrazide in O.2 M cacodylate buffer (pH 6.9) for 30 min . Finally, cells were treated with the reduced OsO4 for 1 h in the darkness and placed 50% ethanol, which was gradually replaced by 70, 90 and 100% ethanol. After this dehydratation, samples were embedded in Epon . After 24-h polymerization at 60 °C, samples were cut using Leica FC6 ultramicrotome (Leica, Wien, Austria) and examined in Tecnai 20 transmission electron microscope (FEI, Endhoven, The Netherland) .
Mitotracker staining and confocal microscopy
C2 cells were plated in 100 mm Petri dishes (2 × 106 cells/well), incubated for 18 h before treatment with 50 or 100 μM 4-IPP (24 h) or with 5 mM metformin (120 h). The cells were stained with MitoTracker Deep Red FM (Molecular Probes, Invitrogen, Carlsbad, CA, USA) at a final concentration of 60 nM, then fixed with 4% paraformaldehyde at 37 °C for 15 min, and washed with phosphate-buffered saline. Immunofluorescence staining was performed on 2-μm paraffin-embedded sections, deparaffinised in xylene and rehydrated in graded alcohols. The slides were washed in 0.05 M phosphate-buffered saline, incubated with DAPI 1:35,000 (Molecular Probes) for 10 min, washed again in 0.05 M phosphate-buffered saline and then fixed using Prolong Antifade (Molecular Probes). Confocal laser scanning microscopy was performed using the Leica TCS SP8 X microscope (Leica Microsystems GmbH, Mannheim, Germany).
3D structures, IHC profile and LGR5 expression of the organoids
In-phase contrast microscopy showed both tubular-branched and more round shaped 3D structures present in C1, while C2 was mainly composed of round-shaped cellular aggregates (Additional file 2: Figure S1).
Taking advantage from the serum-free growth conditions of CRC-pc organoids, we profiled the secretome compartment to search for novel molecular candidates for therapy involved in CRC-pc development and coupled it with a classical pharmacological approach aimed at exploring the possible implications of these candidates in CRC-pc. Indeed, we also used C1 organoids for validating the results obtained from the use of C2.
We stated that these proteins playing a role in crucial biological processes were secreted by organoids and that they were present also in clinical samples. These studies support the concept that CRC-pc organoids may constitute a pre-clinical model for investigating the biology of CRC-derived peritoneal lesions.
Over-represented biological processes identified by secretome in C2 organoids
Analysis of the secreted proteins with annotations in the IPA database identified networks that were enriched in proteins involved in metabolism homeostasis, protein ubiquitination, cell cycle and DNA repair, and were significantly over-represented in cancer (Additional file 2: Figure S2).
Macrophage migration inhibitory factor (MIF)/CD74 signalling axis
Secretome composition of C2 organoids included proteins potentially able to mediate high metabolic demand, adaptive homeostasis along with enhancing stress resistance. One of them was the multifunctional cytokine MIF (Fig. 3c), the ligand of CD74 receptor. MIF/CD74 axis can promote cell survival by modulating glucose uptake and metabolism through the activation of AKT and AMPK proteins and is considered a potential target for therapy  (Fig. 3c).
Since MIF/CD74 axis through AMPK activation accelerates glucose uptake, which enhances mitochondrial functions , we assessed whether the MIF/CD74 axis supports and maintains high levels of metabolism of C2 organoids. We have recently observed an extensive alteration of some crucial oncogenic signals and a decrease in Krebs cycle activity through the specific inhibition of MIF activity using 4-IPP in papillary and anaplastic thyroids carcinoma models . In the work we demonstrated by MALDI-TOF analysis that 4-IPP can effectively recognize MIF as its target.
We expect that targeting MIF/CD74 axis in CRC-pc models could give similar results inducing a strong impairment in many crucial metabolic pathways and leading to a dramatic change of the homeostasis of colonic carcinomatosis. Conversely, we examined the effects of AMPK stimulation by using metformin, an AMPK activator that disrupts mitochondrial functions through inactivating mitochondrial respiratory chain complex I .
Cellular and signalling effects of 4-IPP and Metformin on C2 organoids
We evaluated the 4-IPP effects by targeting C2 organoids with various concentrations of inhibitor (10, 25, 50, 100 μM). Twenty-four hours after treatment with 4-IPP, C2 organoids appeared disaggregated (Fig. 4c left) and died within 48 h. The disaggregation of organoids was also observed after treatment with metformin that, on the other hand, induced only a slight increase of cell death after 120 h (Trypan blue assay, Fig. 4d).
Treatment with 50 and 100 μM 4-IPP activated ERK phosphorylation. In contrast, AKT and AMPK phosphorylation was abrogated (Fig. 4e). The decreased phosphorylation of the AKT-specific phosphorylation site on FOXO3 further demonstrated the suppression of AKT activity and possibly supported the impairment of C2 viability. Shorter 4-IPP treatments (3, 6 and 12 h) exhibited similar results (Additional file 2: Figure S3). Treatment of C2 organoids with metformin inhibited phosphorylation of mTOR, ribosome protein S6 and 4E-BP1 but did not inhibit ERK and AKT (Fig. 4f). Treatments with 4-IPP increased the activity of the stress-activated protein kinase, JNK, in a dose-dependent manner, explainable by the activation of a complete stress-related response (Fig. 4e). In parallel, a dramatic change in the anti-phosphotyrosine/phosphothreonine profile was observed probably due to inhibited phosphatase activities (Fig. 4g, left panel). Indeed, PP2A phosphorylation was switched off after 4-IPP treatment (Fig. 4h, left panel). Conversely, metformin treatment did not significantly modify phosphotyrosine/phosphothreonine profiles and phosphorylation of PP2A and PPP1A (Fig. 4g, and h, right panels).
These results suggested that inhibition of AKT and AMPK-related pathways has more pronounced effects in terms of cell survival and stress-related response rather than the implementation of AMPK/mTOR/S6/4EBP1 axis (Fig. 4i).
Metabolic changes after 4-IPP and metformin treatments
Mitochondria impairment after 4-IPP and metformin treatments in C2 organoids
A mitochondrial-targeted probe which accumulates in mitochondria, depending on their membrane potential, was used to morphologically explore the mitochondrial network in C2 organoids under 4-IPP and metformin inhibition. Briefly, we monitored the mitochondrial membrane potential using JC1 probe, a cationic carbocyanine fluorescent dye that exhibits a potential-dependent accumulation in mitochondria: a fluorescent emission shift from green (~525 nm) to red (~590 nm) indicates increase of the membrane potential, while a decrease in the red/green fluorescence intensity ratio highlights mitochondrial depolarization. Our analyses showed that mitochondria were distributed broadly in the cytoplasm and characterized by a perinuclear punctuated network in untreated cells (Fig. 6b). Cells treated with 4-IPP showed mitochondria with an altered morphology indicated by changes in immunofluorescence staining patterns. Mitochondria appeared much less tubular and a diffuse cytosolic pattern of fluorescence was observed. Of note, treated cells also showed signs of nuclear destruction (Fig. 6b, left). Metformin treatment decreased the fluorescence of the probe and several cells displayed a negative fluorescence signal (Fig. 6b, right), indicating a clear loss of mitochondrial membrane potential, which is an important indicator of functional mitochondria. The results highlighted a mitochondrial depolarization after metformin treatment (Fig. 6c).
Using electron microscopy to examine the morphology of mitochondria in C2 organoids treated with 4-IPP, we observed signs of necrosis, including strong condensation of chromatin along a nuclear envelope. There, mitochondria were smaller than in non-treated cells with significant impairment of their structure. The number of lipid droplets in cytosol was smaller than in cells treated with metformin (Fig. 6D1-D3). In organoids treated with metformin, we found many large mitochondria with irregular contours and a modest number of cristae. These mitochondria contained multi-lamellar structures inside, and were aligned with residual lipid droplets accumulated inside the cytosol (Fig. 6D4-D6).
These results suggested that ROS production likely due to the loss/reduction of mitochondrial activity affected viability of C2 organoids (Fig. 6e). Specifically, 4-IPP treated C2 organoids showed autophagy structures (Fig. 6d) that are associated with necrosis and cell death.
4-IPP and metformin effects are recapitulated also in the C1 organoids
We explored the opportunity of using data from the secretome analysis of patient-derived cancer organoids established from two peritoneal carcinomatosis (C1 and C2), to identify possible targets for therapy. The analysed organoids presented self-renewal capacity, the ability to form the typical 3D structure, and a significant positivity for stem biomarkers, as shown by the number of highly-dividing LGR5+ CSCs, especially in C2 organoids. LGR5+ cells are believed to be fast-cycling and resistant to irradiation and chemotherapy and have been shown to initiate intestinal organoid growth in a 3D culture system when isolated from the mouse small intestine [8, 26]. This high proliferation suggests that LGR5+ cells are adapted to facilitate the uptake and incorporation of nutrients into the biomass (nucleotide, amino acids and lipids) needed to generate new cells . Remarkably, this adaptation is not merely due to in vitro growth conditions but was a characteristic already present in the original tumours, both presenting a high number of LGR5+ cells and high mitotic index.
Accordingly, GO Analysis of the secretome profile of the fastest growing C2 organoids revealed prominent expression of metabolic pathways related to oxidative homeostasis, glucose metabolism, and the major glucose catabolic pathway (pentose phosphate pathway) that links glucose metabolism to biosynthesis of the nucleotide precursor ribose, coordinating glucose flux and supporting the cellular biogenesis of macromolecules and energy production .
The simultaneous positivity of the two organoids for MIF suggests the rationale for inhibition of MIF/CD74 signalling axis, which is known to support AMPK activation, glycolysis, oxidative phosphorylation, but also to compensate for the effects of high glucose oxidation . AMPK activation enhances both the transcription and translocation of Glut4 with a consequent increase in glucose uptake, which in turn activates the PI3K/AKT pathway . Activated AMPK is also responsible for initiating alternative energy-generating processes such as fatty acid oxidation . The activation of AMPK and the subsequent glycolytic switch observed in mitotic cells supports the possibility of a dependence on energy pathways to survive in mitosis . AMPK senses ATP loss and enhances glycolysis to protect from death. Previous research has shown that MIF acts through the AMPK signalling pathway to induce cellular resistance to glucose deprivation, ischemia, hypoxia, oxidation and stress senescence .
Our results support the concept that CSCs, through the expression of MIF and CD74, become protected by energy-default processes which force cancer cells with defective mitochondria to generate energy through an AMPK-regulated glycolysis in the cytoplasm . Thus, the inhibition of AMPK signalling through the suppression of MIF/CD74 signalling could be a rational strategy that affects the special energetic requirements of C1 and C2 organoids.
Indeed, knocking down MIF/CD74 signalling through 4-IPP decreased SOD1 and resulted in changes in mitochondrial morphology and mass. An increase of ROS produced a JNK mediated stress response (Fig. 4). The oxidative shift in the redox conditions reduced phosphatases activity, blocking signal propagation in the cell through a number of signalling pathways involving protein kinases .
In both organoids, the inhibition of AMPK-mediated signalling is associated with the inactivation of both AKT and FOXO3. Of note, FOXO3 can induce a number of genes that protect against ROS suggesting that it plays a role in keeping cellular ROS low. JNK activation resulted after treatment, possibly modulating cellular response to ROS independent of changes in the intracellular AMP level  and likely inducing a defective autophagic process followed by rapid cell death.
ROS increase is also the cause of the observed inactivation of PP2A phosphatase and of the relevant consequences in terms of signal transduction response. Inhibition of ERK1/2 dephosphorylation and the general inhibition of protein dephosphorylation observed after treatment support this interpretation of the results.
However, redox regulation of phosphatases is poorly understood. Protein phosphatases are inhibited by ROS, which target specific redox sensitive amino acids, but PP2A catalytic activity leading to the activation of cellular stress signalling pathways can be also modulated by hydrogen peroxide .
Our findings define a MIF/CD74/AMPK pathway in the colon peritoneal carcinomatosis, for the first time elucidating a signal transduction mechanism between autocrine/paracrine factors and AMPK activation. The results provide initial proof-of-concept that pharmacologic treatment blocking MIF/CD74 signalling pathways disrupts energy homeostasis in CRC-pc derived organoids, in vitro, by inducing cell death.
Our investigations were also aimed to study the effects of metformin, a drug for treating type 2 diabetes, whose use has been associated with decreased cancer risk, and that kills cancer-initiating/stem cells from a variety of cancers with AMPK activation . Metformin is known to inhibit the mitochondrial respiratory chain complex I that reduces ATP production and increases the intracellular ratio of AMP/ATP, resulting in AMPK activation that switches cells from an anabolic to a catabolic state. We found that metformin reprograms organoid metabolism. This process involved both AMPK activation, which reduces mTOR activity and protein translation, and complex I inhibition, which promotes ROS production within the mitochondrial matrix. As an effect of AMPK activation, glycolysis was stimulated, producing a large amount of lactate. Furthermore, the inhibition of complex I promoted superoxide production within the mitochondrial matrix, which provoked dysfunctional mitochondrial swelling, interrupted the tricarboxylic acid cycle and led to a compensatory increase in lactate and glycolytic ATP and aberrant lipid accumulation.
C2 organoids treated with metformin presented dramatic changes in mitochondria morphology – deformation and partial loss of mitochondrial membranes and degradation of cristae. Consequently, we observed accumulation of free radicals and loss of membrane potential. These effects could be explained by the ability of metformin to induce mitochondrial depolarization and increase ROS through inhibition of complex I , which also leads to mitochondrial cristae degradation . Loss of mitochondrial function limits the production of lipids, nucleotides and amino acids used by cells for the creation of new biomass, and could explain the inhibited cell proliferation after treatment with metformin, as suggested by the reduced number of disaggregated cells counted in treated samples during the trypan blue assay (data not shown).
In conclusion, 4-IPP and metformin have profound effects on the metabolism of organoids derived from CRC-pcs. Interestingly, C1 and C2 organoids presented different phenotypic features, but similar responses when treated with 4-IPP or metformin – activation of stress-signalling pathways and cell death with 4-IPP treatments; inhibition of mitochondria, oxidation of glucose and lipids resulting in energy restriction with metformin treatments.
We have previously shown that inhibition of MIF/CD74 signalling axis blocks thyroid cancer cells growth by inducing cell death during mitosis . Other studies have demonstrated the efficacy of MIF or CD74 targeting in several cancers providing a rationale for the development of therapeutic agents and clinical trials to study the effects of inhibiting a newly discovered MIF isoform (oxMIF) on different cancers, including metastatic CRC (NCT01765790). Milatuzumab, the first anti-CD74 antibody that has entered into clinical tests, is currently being studied for the treatment of non Hodgkin lymphomas, chronic lymphocytic leukemia, and multiple myeloma [33, 38] and could be potentially tested in MIF/CD74 positive CRC-pc.
MIF inhibitors, particularly when acting on the MIF/CD74 axis, could be a very attractive strategy for cancer therapeutic intervention due to the nonphysiologic enzymatic activity of the cytokine that is evolutionary well-conserved . MIF belongs to the family of tautomerase proteins and can catalyze the tautomerization of nonphysiologic substrates, such as D-dopachrome and L-dopachrome methyl ester, into their corresponding indole derivates. This peculiar feature seems to be mediated by the NH2-terminal Proline of MIF (Pro-1) and strategies based on targeting Pro-1 are able to abrogate the tautomerase activity . Indeed, different works have shown that the development of small molecules antagonist of the MIF enzymatic active site could be an effective strategy to abrogate its functions. Winner and colleagues showed how 4-IPP serves as suicide substrate for MIF, resulting in the covalent modification of Pro-1 . Exposure to 4-IPP decreased MIF immunoreactivity and similar results were also recapitulated using MIF silencing-based strategies . Some recent works showed how 4-IPP interferes with several activities peculiar of MIF, such as neutrophil lung recruitment , the maintenance of a chemoresistant phenotype  and the reprogramming of tumor associated macrophages that supports malignant plasma cell survival and resistance to therapy in multiple myeloma cells .
Moreover, MIF inhibitors, particularly in conjunction with CD74 inhibition, could be very efficient in blocking CRC-pc progression. The systemic effects of inhibitors that interfere with energy metabolism are still only partially known, however ongoing clinical studies seem to give encouraging results.
Differently, metformin is widely used with mild or no side effects, and therefore the effects of energetic reduction induced by metformin on organoids could be combined with drugs which can act in synergy and induce cell death.
Our study shows that the modulation of AMPK function, both through its activation by metformin, or its reduction caused by the removal of MIF/CD74 signalling axis, is critical for maintaining cell energy balance of CRC-pc. Metformin elicits the metabolic reprogramming by decreasing oxidative phosphorylation and increasing dependency on glycolytic metabolism. Conversely, inhibition of MIF/CD74 signalling axis elevated ROS rendering cancer cells vulnerable to oxidative stress-induced cell death. In conclusion, targeting the metabolism of cancer cells opens new lines of research that could lead to the design of new therapies for the treatment of CRC-pc.
Colorectal cancer peritoneal carcinomatosis organoid 1
Colorectal cancer peritoneal carcinomatosis organoid 2
Colorectal cancer peritoneal carcinomatosis organoid 3
Colorectal cancer peritoneal carcinomatosis organoid 4
Colorectal cancer peritoneal carcinomatosis organoid 5
Colorectal cancer peritoneal carcinomatosis
Cancer Stem Cells
Fatty acids synthesis
False discovery rate.
Formalin Fixed Paraffin Embedded
Isotope-dilution gas-chromatography mass spectrometry
Haematoxylin and eosin
in situ Hybridization
Nano-scale liquid-chromatography tandem mass spectrometry
Leucine-rich repeat-containing G-protein coupled receptor 5
Macrophage Migration Inhibitory Factor
Nicotinamide adenine dinucleotide phosphate
Oxidized Macrophage Migration Inhibitory Factor isoform
Protein Analysis Through Evolutionary Relationships
Reactive Oxygen Species
Sodium dodecyl sulfate
Search Tool for the Retrieval of Interacting Genes/proteins
Tricarboxylic acid cycle
We thank Dr. Francesco Gallino for providing us surgical specimens of the colorectal peritoneal carcinomatoses, Dr. Maria Di Bartolomeo and Dr. Filippo Pietrantonio for critical discussions on treatment of the colorectal peritoneal carcinomatoses and Patrizia Casalini for confocal microscopy analyses.
This work was supported in part by a grant [No. 14487] to MA Pierotti from AIRC (Associazione Italiana Ricerca Cancro), by the Italian Ministry of Public Health and by funds obtained through an Italian law that allows taxpayers to allocate 0.5% share of their income tax contribution to a research institution.
Availability of data and materials
The datasets of proteins and metabolites generated and/or analyzed during the current study are available from the corresponding author on reasonable request.
FB, AM, LV, IB and MG, conceived and designed the study. FB, AM, LV, AB, CCV, CC, VL, GVB, AAM, MM, GM, AG and EL collected and assembled data. FB, AM, LV, IB and MG, wrote the manuscript. MAP and SP critically reviewed the manuscript. All authors analyzed and interpreted the results. All authors reviewed the manuscript before submission. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study was approved by the Institutional Review Board of Fondazione IRCCS Istituto Nazionale dei Tumori, and each patient provided written informed consent to donate remaining tissues after diagnostic procedures.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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