Original articles
Published: 2023-10-09
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Up-regulation by overexpression of c-MET in fibroblastic foci of usual interstitial pneumonia

Fondazione Poliambulanza
Respiratory Diseases Unit, Carlo Poma Hospital, Azienda Territoriale Socio Sanitaria (ATS) of Mantova, Mantova, Italy
Operative Unit of Pathologic Anatomy, Azienda USL-IRCCS Reggio Emilia, Reggio Emilia, Italy
Operative Unit of Pathology, Diagnostic Services Area, Fondazione Poliambulanza Hospital Institute, Brescia, Italy
Operative Unit of Oncology, Azienda USL Valle d’Aosta, Aosta, Italy
Operative Unit of Pathologic Anatomy, Azienda USL-IRCCS Reggio Emilia, Reggio Emilia, Italy
Operative Unit of Pathology, Diagnostic Services Area, Fondazione Poliambulanza Hospital Institute, Brescia, Italy
UIP IPF fibroblast foci c-MET immunohistochemistry PCR

Abstract

Background. Usual interstitial pneumonia (UIP) is the radiologic and histologic hallmark of idiopathic pulmonary fibrosis (IPF) and the commonest histologic pattern of other progressive fibrosing interstitial lung diseases (e.g., fibrotic hypersensitivity pneumonia). Analogous to lung cancer, activation of epithelial-to-mesenchymal transition (EMT) is one of the main molecular pathways recently identified by transcriptomic studies in IPF. Fibroblastic foci (FF) are considered the active/trigger component of UIP pattern. The proto-oncogene C-MET is a key gene among molecules promoting EMT against which several inhibitors are currently available or promising in ongoing studies on lung cancer.
Methods. Twenty surgical cases of diffuse fibrosing interstitial lung diseases (fILD) with UIP pattern and FF-rich (17 IPF and 3 patients with fibrotic hypersensitivity pneumonia, fHP) were retrospectively selected. FF were manually microdissected and analysed for c-MET gene alterations (FISH amplification and gene hot-spot mutations Sanger sequencing) and tested with a c-MET companion diagnostic antibody (clone SP44 metmab) by immunohistochemistry.
Results. FF are characterized by upregulation of c-MET as shown by overexpression of the protein in 80% of cases, while no gene amplification by FISH or mutations were detected. C-MET upregulation of FF was observed either in IPF and fHP, with a tropism for the epithelial cell component only.
Conclusion. Upregulation of c-MET in FF of ILD with UIP pattern further confirms the key role of the proto-oncogene c-MET in its pathogenesis, possibly representing an interesting and easily-detectable molecular target for selective therapy using specific inhibitors in future clinical trials, similar to lung cancer. It is reasonable to speculate that molecular alterations in FF can also be detected in FF by transbronchial cryobiopsy. Key words: UIP, IPF, fibroblast foci, c-MET, immunohistochemistry, PCR.

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Introduction

Idiopathic pulmonary fibrosis (IPF) is a chronic, irreversible and progressive, diffuse fibrosing lung disease defined by the radiologic and histologic pattern of usual interstitial pneumonia (UIP), the most common pattern among idiopathic interstitial lung diseases 1,2.

IPF has a lethal outcome with more than 50% of patients dying within 3 years from diagnosis 2-4. The disease ultimately leads to extensive scarring changes of the pulmonary parenchyma through activation of a complex crossing of several pathways, including extracellular matrix degradation, angiogenesis, lung senescence and Wnt signaling, non-coding RNA (miRNAs), inflammation and apoptosis among others 3-4. The dramatic fibrogenic process substituting the alveolar ventilated lung parenchyma is thought to be triggered by chronic alveolar epithelial injuries 2-7, such as smoke, exposure to organic and inorganic toxic agents interplaying in a genetic background increasing the risk of disease, although the cause of IPF remains elusive and its pathogenesis incompletely understood.

Histologically, UIP pattern of fibrosis is defined by a patchwork appearance resulting from abrupt alternating areas of scarred and normal lung, architectural distortion with/without honeycombing change and fibroblastic foci 2,8.

This complex network of mechanisms is variably involved in the pathogenesis of IPF, but also in other diffuse fibrosing lung diseases leading to UIP pattern, mainly fibrotic hypersensitivity pneumonia (fHP) and collagen vascular diseases 2-6. The impact of molecular studies in the last years is limited by the investigation of bulk tissue comprising various lung compartments and cell types, while novel molecular applications aimed at analyzing single targets and microenvironmental components on human tissue appear to unveil new promising molecular data that could lead to better comprehension of the pathogenetic mechanisms involved in IPF as well as alternative and more effective treatments guided by a targeted approach 7-14.

In this setting, FF are usually seen at the interface between densely fibrotic and relatively normal-appearing lung parenchyma 14,15. FF are considered the active component and progressing front of UIP pattern finally leading to “end-stage” fibrotic destruction of the lung parenchyma architecture and are thought to be more likely derived from the transformation of alveolar epithelial cells covering the FF through epithelial-to-mesenchymal transition (EMT) phenomenon. EMT is due to the loss of epithelial cell-cell adhesion molecules (e.g., E-cadherin) and concomitant gain of mesenchymal markers (e.g., N-cadherin, alpha-smooth muscle actin) 7,10,11-14.

The well-established role of EMT in the pathogenesis of IPF is supported by the expression of driving transcription factors, such as SNAIL1, SNAIL2 (SLUG), TWIST1, ZEB1, ZEB2 (SIP1), PRRX1 and Goosecoid repressing the molecules of cell-cell adhesion through the activation of signaling pathways that can induce EMT, such as transforming growth factor-beta (TGF-β) 12-14.

The up-regulation of epithelial–mesenchymal transition (EMT) in IPF is further supported by Chilosi et al. 13 who studied the immunohistochemical and immunofluorescent expression of ZEB1, Tubβ3, and β-catenin in all tissue samples from 34 idiopathic pulmonary fibrosis cases that were concurrently expressed in fibroblastic foci, damaged epithelial cells overlying active fibrosis and in pericytes within neo-angiogenesis areas. These results were also confirmed by immunofluorescence assay, indirectly supporting miR-200 deregulation and EMT activation in IPF. The abnormal expression and localization of these proteins in bronchiolar fibro-proliferative lesions is unique for idiopathic pulmonary fibrosis, and might represent a disease-specific marker in challenging lung biopsies.

Again, according to Yamaguchi et al. 14, FF are more likely derived from the epithelial-to-mesenchymal transitioned alveolar epithelia located over them. On the basis of these findings, inhibition of transforming growth factor-β signaling, which can suppress EMT of the alveolar epithelial cells in vitro, is a potential strategy for treating IPF.

Among molecules involved in EMT, deeply investigated in various neoplasms, MET acts as a receptor tyrosine kinase (RTK) and is part of a larger family of growth factor receptors 15-19.

Hepatocyte growth factor (HGF), the ligand of MET, is a member of the plasminogen-related growth factor family that promotes apoptosis of myofibroblast and inhibition of epithelial-to-mesenchymal cell transition (EMT). HGF binding to MET results in receptor homodimerization and phosphorylation of tyrosine residues located in the kinase domain. This causes activation of the mitogen-activated protein kinase (MAPK) cascades, leading MAPK translocation to the nucleus thus activating transcription factors responsible for regulating a large number of genes resulting in cell proliferation, cell motility, cell cycle progression, invasion and transformation 15-19. Thus, HGF acts as an anti-fibrogenic molecule, but its receptor MET is considered to have a key role in promoting EMT transition both in pulmonary fibrosis and lung cancerogenesis 16,18.

Vukmirovic et al. 19 recently demonstrated a significant increase of c-MET mRNA in a study of large scale genome transcript profiling using RNA sequencing (RNA-Seq) applied to archived formalin-fixed paraffin-embedded (FFPE) IPF tissues. The authors compared 7 cases of IPF with 5 control lung tissue, performing a 50-base paired-end sequencing on Illumina 2000 Hiseq. In the study, 4,131 genes were differentially expressed between IPF and controls (1,920 increased and 2,211 decreased). Pathway enrichment analysis performed using MetaCore confirmed numerous IPF relevant genes including TGF-β WNT, and those involved in extracellular remodelling and regulation of EMT transition. The study notably demonstrates that sequencing of RNA obtained from archived FFPE lung tissues is feasible, since results obtained from FFPE tissue were highly comparable to fresh frozen tissues.

The ability to perform RNA-Seq on archived FFPE IPF tissues greatly enhances the availability of tissue biopsies for molecular investigations in IPF.

Since FF indicate the site of starting of the disease and represents the pathognomonic histologic modification in the pathogenesis of the pulmonary fibrotic disease with UIP pattern 7,10,11, some researchers have designed studies to specifically microdissect FF and then analyze tissue by gene expression profiling.

In particular, Guillotin et al. 7 first performed a transcriptomic analysis in FF isolated from lung tissue of IPF by laser capture microdissection with identification of clusters of genes associated with cell cycle, inflammation/differentiation, translation and cytoskeleton/cell adhesion. The authors showed that transforming growth factor β1 (TGF-β1), RhoA kinase and the TSC2/RHEB axis formed major signalling targetable clusters associated with collagen gene expression in lung fibrosis and other fibrotic conditions including cancer-associated fibroblasts. While microdissected FF in the study by Guillotin and colleagues included only the mesenchymal myofibroblastic proliferation without the epithelial component, in a subsequent study Kamp et al. 10 microdissected and analyzed the entire sandwich (mesenchymal and epithelial components) of FF in IPF (6 cases) and chronic fibrotic sarcoidosis (6 cases) by gene expression signature evidencing upregulation of several genes, including c-MET.

Similarly, Calabrese et al. 11 used the same approach in a study on microdissected FF (entire sandwich) from 12 IPF (10 lung transplantations and 2 diagnostic VATS). The authors found 23 up-regulated genes compared with normal lung from spontaneous pneumothorax, mainly related to epithelial cell adhesion (high molecular weight cytokeratins, desmocollin-3, CEACAM 5-7), cell migration/EMT (MET), senescence, programmed cell death (Serpine1) and secretory mucin proteins (MUC5AC, MUC5B).

Since FF share several pathogenetic mechanisms with lung cancer, including EMT upregulation, and the proto-oncogene c-MET is a druggable receptor tyrosine kinase against which promising inhibitors are still available and ongoing, the aims of this study were the following: i) to demonstrate the feasibility of microdissection of FF using a manual, light microscope-guided approach, enabling; ii) extractive molecular analysis of DNA alterations focused on investigation of one of the main genes involved in EMT pathway, namely the proto-oncogene c-MET (FISH amplification and gene mutations in the most important hot spots) in FF; iii) the product of c-MET gene was analyzed in FF by immunohistochemical expression using a companion diagnostics test (CDx anti-total met clone SP44 metmab, Ventana/Roche) performed for lung cancer 20.

Materials and methods

Twenty cases of diffuse fibrosing interstitial lung disease with UIP pattern (17 IPF, 3 fibrotic HP) were selected for the study. The cases were from routine practice and consultation archive of one of the authors (GR) diagnosed between January 2013 and October 2017. All patients had a definitive diagnosis established through multidisciplinary review of clinical, radiological, and pathological data, according to the last criteria of international Guidelines 1,2.

The study was approved by local Ethical Committee (code RE14790). All patients ultimately died and the patient’s consensus was obtained from the Privacy Authority. All information regarding human material was anonymously managed through numerical code identification. All samples were handled in compliance with the Helsinki Declaration ().

The UIP pattern was histologically confirmed on lung tissue obtained from surgical biopsy using a video-assisted thoracoscopic approach. All lung specimens were formalin-fixed for at least 14 and no more than 24 hours, then entirely sampled after removal of the metallic staples at the resection margins, and slices obtained with perpendicular sections on the long axis of the specimen were then paraffin-embedded. From each paraffin block, 4-μm thick sections were obtained and routinely stained with hematoxylin-eosin for examination at light microscopy. For in situ (immunohistochemistry, FISH) and extractive molecular analysis, only paraffin-embedded blocks containing at least 10 FF x slide were selected.

With FF we considered the scattered, tiny structures composed of a micronodular aggregate of fibroblasts/myofibroblasts lined by metaplastic epithelial cells (Fig. 1) (so-called epithelial/myofibroblastic sandwiches).

The availability of a sufficient number of fibroblastic foci was then a prerequisite to enter in the study, since this specific finding was the target of molecular studies.

IMMUNOHISTOCHEMISTRY (IHC)

The IHC evaluations were performed using the rabbit monoclonal primary antibody anti-total c-MET (clone SP44, Ventana Medical Systems, Roche, prediluted) revealed using an UltraView Universal DAB Detection Kit (Ventana Medical Systems, Tucson, AZ). The IHC staining procedure was carried out according to the manufacturer’s instructions using the ULTRA automated immunostainer (Ventana BenchMark Ultra). The IHC staining was evaluated by 2 pathologists according to modified MetMab criteria 17,20.Accordingly, FF were considered as MET positive when strong MET membranous and/or cytoplasmic staining (2 + or 3+) was noted in more than 50% of epithelial and\or mesenchymal cells. Finally, a case was rated as positive or MET overexpressed when at at least 50% of examined FF in immunotested slides were positive.

FISH analysis

FISH evaluation of MET was performed using unstined FFPE tumor tissue sections, as elsewhere described 21. FISH analysis was performed using the ZytoLight SPEC MET/CEN 7 Dual Color Probe (PL46) (Bio-Optica, Milan, Italy), according to the manufacturer’s instructions. It should be noted that a minimum of 50 non-overlapping epithelial and/or myofibroblastic cells comprised in the FF with hybridization signals were analyzed in each sample under a fluorescence microscope (BX51, Olympus, Tokyo, Japan).

MET amplification was recorded by estimating the ratio between the number of MET copies and the copies of the chromosome 7 centromere (CEP7) according to Ding et al. 21. Mean cMET/CEP7 ratio was calculated for each probe by scoring the number of c-MET and CEP7 each nucleus independently. MET copy number ≥ 5 and/or MET:CEP7 signal ratio ≥ 2 were considered as amplification. In contrast, MET:CEP7 ratio of < 2 was classified as non-amplified MET. While patients with MET copy numbers of ≥ 5 but a ratio of < 2 were classified as MET gain, both MET and CEP7 copy numbers of ≥ 3 but < 5 were classified as MET polysomy 21.

MOLECULAR ANALYSIS

Five-µm thick sections obtained from a representative paraffin-embedded block were deparaffinized using xylene, and tumor DNA was extracted manual microdissection method under the guide of a light-microscope (Leica DM750 with incorporated ICC50W camera, Buccinasco/Milan, Italy). Manual microdissection of fibroblast foci with overlying alveolar pneumocytes was at 100X magnification (objective X10) on hematoxylin-eosin-stained slides without coverslip using a sterile needle (27 G, Agani Needle, Terumo Europe, Hamburg, Germany). At least 50 fibroblast foci per case were dissected and placed into a sterile Eppendorf tube (Fig. 2). Microdissected cells were then processed as previously described 22. The forward and reverse oligonucleotide primers used to amplify c-MET exons are listed in Table I.

STATISTICAL ANALYSIS

Statistical calculations with comparison of categorical variables were performed using the chi-square statistic with the Fisher exact test P values.

Results

The case series consisted of 20 patients with diffuse fibrosing interstitial lung disease with UIP pattern at histology, classified as IPF (n = 17) and fibrotic hypersensitivity pneumonia (fHP, n = 3) after multidisciplinary discussion, in agreement with the most recent international guidelines 1,2.

There were 15 males (75%) and the median age was 66 years (range, 54-80 years).

At the time of diagnosis, 45% of patients were stable, while 11 were in progression.

The main clinicopathologic data of the series is summarized in Table II.

No significant differences were observed when the variables were matched by statistical analysis.

IMMUNO-MOLECULAR DETERMINATIONS

Direct Sanger sequencing of microdissected FF did not show mutations in the c-MET exons investigated (Fig. 3).

FISH analysis performed for c-MET gene amplification did not reveal increased copies of the gene (Fig. 4).

Immunohistochemical expression of MET protein using the total MET monoclonal cDx SP44 (metmab) evidenced overexpression in 80% of the cases, 82.3% (14 of 17) in IPF and 66.6% (2 of 3) in fHP.

Of note, MET overexpression is noted in the epithelial cells of FF, but not in the mesenchymal component (Fig. 5).

No significant expression was identified in any other tissue compartment of the lung.

No significant differences were observed when the variables were matched by statistical analysis.

Discussion

Fibroblastic foci (FF) are one of the main histologic hallmarks of ILD with UIP pattern, either in IPF and secondary UIP, such as fibrotic hypersensitivity pneumonia 2-4,6,14. FF are considered the active/trigger component of UIP, possibly resulting from chronic injuries to the alveolar epithelial cells leading to mesenchymal activation with localized proliferation of fibroblast/myofibroblasts 2-4,6,7,10,11,14. The numerosity of FF in UIP is directly correlated to disease progression and poor outcome 2-4. FF interestingly represent a tissutal compartment of UIP characterized by the activation of epithelial-to mesenchymal transition (EMT), as recently demonstrated in various studies 7,10,11,13,14. Chilosi et al 13. provided robust evidence that Tubβ3, ZEB1 and β-catenin, target proteins of the miR-200-family, are abnormally expressed at sites of damage and repair in IPF, with specific localization in FF and epithelial cells of honeycombing changes. As already suggested, ZEB1 is a crucial activator of epithelial to mesenchymal transition, and its expression in epithelial cells is triggered by different signaling pathways and transcription factors, including Wnt-β catenin, TGFβ, and Twist, all molecules upregulated in IPF 3,4,14.

Of note, aberrant up-regulation of the proto-oncogene c-MET is emerged in several transcriptomic studies on mRNA in IPF 7,8,10,11,19. c-MET is considered an important actionable target in many solid tumors 18,20-23; therefore, biomarker discovery becomes essential in order to guide clinical intervention and patient stratification with the aim of moving towards personalized medicine.

MET, a high affinity tyrosine kinase receptor for hepatocyte growth factor (HGF, also known as scatter factor) is a disulfide-linked heterodimer made of 45 kDa α- and 145 kDa β-subunits (1,2). The α-subunit and the amino-terminal region of the β-subunit form the extracellular domain. The remainder of the β-chain spans the plasma membrane and contains a cytoplasmic region with tyrosine kinase activity. Interaction of MET with HGF results in autophosphorylation at multiple tyrosines, which recruits several downstream signaling components, including Gab1, c-Cbl, and PI3 kinase 15-18,23. These fundamental events are important for all of the biological functions involving MET kinase activity. Phosphorylation at Tyr1234/1235 in the Met kinase domain is critical for kinase activation 15-18, whereas phosphorylation at Tyr1349 in the Met cytoplasmic domain provides a direct binding site for Gab1. Research studies have shown that altered MET levels and/or tyrosine kinase activities are found in several types of tumors, including renal, colon, and breast cancer 16-18,23. Thus, investigators concluded that Met is an attractive potential cancer therapeutic and diagnostic target 23.

Immunohistochemical evaluation demonstrated that hyperplastic alveolar type II epithelial cells, as well as alveolar macrophages, were strongly stained with anti-HGF antibody in tissues of patients with IPF. The concentration of HGF in bronchoalveolar lavage fluid (BALF) was significantly higher than in normal controls (0.23 +/- 0.09 pg/microg) in patients with IPF (0.77 +/- 0.88 pg of HGF/microg of albumin, P < 0.001), lung fibrosis associated with rheumatoid arthritis (0.50 +/- 0.64 pg/microg, P < 0.01), and sarcoidosis (0.41 +/- 0.61 pg/microg, P < 0.05) 15-18. In situ hybridization revealed mRNA for HGF in alveolar macrophages (especially small monocyte-like macrophages). These results indicate that the increase in HGF in peripheral air spaces is due to augmented HGF production by alveolar epithelial cells and alveolar macrophages. HGF, through a paracrine mechanism, may play an important role in the repair and healing of the inflammatory lung damage in pulmonary fibrosis 15,18.

Therefore, there is a consistent body of evidence to state that EMT pathway involving HGF/c-MET is disrupted in IPF. Although preliminary, the current data further support the role of c-MET as an interesting molecular target in pulmonary fibrosis with UIP pattern.

The original study design here proposed also suggests that clinical trials in IPF may replicate those in lung cancer evidencing druggable molecular biomarkers.

It is of note that promising results have been observed in phase I and II studies using telisotuzumab vedotin, an antibody-drug coniugate targeting c-MET, in monotherapy in advanced non-small cell lung cancer (NSCLC) characterized by overexpression of c-MET using the same metmab companion diagnostic immunohistochemistry clone SP44 with the scoring system adopted for FF here presented 20. Camidge et al. 24. demonstrated that Teliso Vedotin monotherapy was well-tolerated and showed antitumor activity in c-MET positive NSCLC.

Since cryobiopsy is the emerging diagnostic interventional procedure to obtain tissue in IPF, and hence FF are easily recognizable in these samples, selective dissection of FF for DNA/RNA extraction seems entirely feasible in lung tissue from cryobiopsy 25.

Finally, the current and previous similar molecular studies obtaining good-quality DNA/RNA from patients with IPF and other ILD with UIP pattern archived in Pathology Units, should convince researchers to implement molecular studies with different methodologies, also permitting isolation of tissue from specific lung compartments of UIP 7,8,10,11,19. A summary of the main findings and study details of all published works microdissecting FF in IPF or other ILD with UIP pattern are reported in Table III.

Of course, this study has several limitations, as follows: a. this is a retrospective observational analysis including selected cases of ILD with UIP pattern comprising several FF, then excluding similar cases characterized by a limited quantity of FF; b. manual microdissection cannot permit an adequate separation (if of some help) of the epithelial cells from fibroblast/myofibroblast component of FF; c. molecular analysis was focused on a limited number of exons of c-MET gene (although including hotspots); d. all cases were from surgical specimens, while there is a worldwide tendency to limit surgical biopsy procedures in favor of less invasive bronchoscopy approach with transbronchial cryobiopsy.

Conclusions

Upregulation of c-MET in FF of ILD with UIP pattern further confirms the key role of the proto-oncogene c-MET in its, possibly representing an interesting easily-detectable molecular target for selective therapy using specific inhibitors in future clinical trials, similarly to lung cancer. It is reasonable to speculate that molecular alterations in FF can also be detected in FF from transbronchial cryobiopsy.

CONFLICTS OF INTEREST

The authors declared no conflicts of interest with respect to the authorship and/or publication of this article. All the material (text, tables and images) used for the current research article is entirely original and never published elsewhere.

FUNDING

This research did not receive any specific grant from funding agencies in the public, commercial, or not-to-profit sectors

AUTHORS’ CONTRIBUTIONS

GR, LM, AC conceived and supervised the study. GS, GJ and LG conceived and conducted all molecular determinations and GC performed the associated analyses and assisted in characterizing the histological stains and identification of clinical morphologies associated with interstititial lung diseases. LM, GR, GC, AC and wrote the manuscript and all authors revised and approved the final version.

ETHICAL CONSIDERATION

The study was approved by Ethical Committee of Azienda SMN Reggio Emilia (code RE14790). All patients ultimately died and the patient’s consensus was obtained from the Privacy Authority. All information regarding the human material was anonymously managed through numerical codes identification. All samples were handled in compliance with the Helsinki Declaration ().

Figures and tables

Figure 1.A case of IPF with several fibroblastic foci (blue circles) characterized by a superficial layer of epithelial cells (blue arrows) covering the proliferation of fibro/myofibroblastic mesenchymal component (hematoxylin-eosin, magnification x 100).

Figure 2.A case of IPF with several fibroblastic foci before (orange circles) and after (blue circles) microdissection using an hematoxylin-eosin-stained slide without coverslide (hematoxylin-eosin, magnification x 100). Microdissection included all epithelial and mesenchymal components (sandwich) of fibroblastic foci.

Figure 3.Electropherogram of direct Sanger showing of the c-MET exon 14 evidencing a wild type gene.

Figure 4.FISH analysis using a MET/CEN7 dual color probe in epithelial and mesenchymal cells of fibroblastic foci showed a regular < 2 MET/CEN7 ratio.

Figure 5.A case of IPF with fibroblastic foci (A, hematoxylin-eosin staining, magnification x 200) showing overexpression of c-MET (clone SP44) in the epithelial component (indicated by blue hashtags) but not in mesenchymal part (red crosstrees) of fibroblastic foci (immunohistochemistry, magnification x 200) or other lung structures.

Primer name Primer sequence A.T. Product size (bp)
Exon 14 c-MET Forward 5’-TTC TGG GCA CGT GGT CAA AGT-3’ 58°C 282 bp
Reverse 5’-AAT GTC ACA ACC CAC TGA GGT-3’
Exon 17 c-MET Forward 5’-GTA TTC ACT GTT CCA TAA TGA AGT-3’ 55°C 287 bp
Reverse 5’-GAT GGC TGG CTT ACA GCT AGT-3’
Exon 18 c-MET Forward 5’-AAC AGT AGA TGC TTA GTT TAT GCT-3’ 55°C 215 bp
Reverse 5’-AAC AGA TTC CTC CTT GTC ACT T-3’
Exon 19 c-MET Forward 5’-TTC TAT TTC AGC CAC GGG TAA T-3’ 55°C 253 bp
Reverse 5’-ATG AAA GTA AAA GAG GAG AAA CTC-3’
A.T., annealing temperature.
Table I.Oligonucleotide primers used in the study.
Characteristics Cases (n = 20) IPF (n = 17) fHP (n = 3)
N.
%
Age Median, 66 years (range: 54-80 years) 71 65
Gender
• Male 15 75 13 1
• Female 5 25 2 2
Smoking habit
• Current/former 16 69 15 1
• Never 4 31 2 2
Disease
• IPF 17 85
• Fibrotic HP 3 15
HRCT
• Probable 12 60 11 1
• Possible 6 30 5 1
• Indeterminate 2 10 1 1
BAL
• Neutrophilic alveolitis 11 55 11 -
• Lymphocytic alveolitis 2 10 - 2
• Not performed 7 35 6 1
Clinical status at diagnosis
• Stable 9 45 4 5
• Progression 11 55 10 1
FVC
• FVC > 80% 13 65 11 2
• FVC < 80% 7 35 6 1
DLCO
• DLCO > 50% 12 60 11 1
• DLCO < 50% 6 30 4 2
• No DLCO 2 10 2 -
Therapy
• Steroid 9 53.8 6 3
• Steroid/NAC/immunosoppressore 8 38.5 8 -
• Nintedanib 3 7.7 3 -
c-MET molecular analysis
• Wid-type setup. 13 100 - -
• Mutated 0 0
FISH
• Amplification 0 0
• Normal setup 20 100
c-MET overexpression
• Negative 4 20 3 1
• Positive 16 80 14 2
Table II.Summary of the main clinicopathologic characteristics of patients included in the study.
Reference Case series Type of dissection Analyzed material Main results
Guillottin 7 2021 FFPE lung tissue with IPF Laser capture microdissection of myofibroblastic component of FF mRNA Prominent clusters of genes associated with cell cycle, inflammation/differentiation, translation and cytoskeleton/cell adhesion
Kamp 10 2021 FFPE tissue from IPF (6 cases) and fibrotic sarcoid (6 cases) Laser capture microdissection of entire FF sandwiches mRNA Up-regulation of several genes, including c-MET. Different expression of CAT1 and SMURF1 between IPF and sarcoid
Calabrese 11 2022 Laser capture microdissection mRNA 23 up-regulated genes when compared with normal lung from spontaneous pneumothorax, mainly related to epithelial cell adhesion (high molecular weight cytokeratins, desmocollin-3, CEACAM 5-7), cell migration/EMT (MET), /senescence/ programmed cell death (Serpine1) and secretory mucin proteins (MUC5AC, MUC5B)
Current series FFPE lung tissue from IPF (\7 IPF) and fHP (3 cases) Manual microdissection under light microscope of entire FF sandwiches DNA (amplification and hot spots mutations of the proto-oncogene c-MET No genetic alterations of the proto-oncogene c-MET Up-regulation by protein overexpression
Abbreviations: FFPE, formalin-fixed paraffin-embedded; IPF, Idiopathic pulmonary fibrosis; fHP, fibrotic hypersensitivity pneumonia; FF, fibroblastic foci; mRNA, messanger ribonucleic acid; DNA, deoxyribonucleic acid, c-MET, MET protooncogene hepatocyte growth factor receptor.
Table III.Summary of the main molecular findings from studies microdissecting fibroblastic foci in interstitial lung disease with UIP pattern.

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  23. Sontake V, Gajjala PR, Kasam RK. New therapeutics based on emerging concepts in pulmonary fibrosis. Expert Opin Ther Targets. 2019; 23:69-81. DOI
  24. Camidge RD, Morgensztern D, Heist RS. Phase I study of 2- or 3 week dosing of telisotuzumab vedotin, an antibody-drug conjugate targeting c-met, monotherapy in patients with advanced non-small cell lung carcinoma. Clin Cancer Res. 2021; 27:5781-5792. DOI
  25. Cooper WA, Mahar A, Myers JL. Cryobiopsy for identification of usual interstitial pneumonia and other interstitial lung disease features. Further Lessons from COLDICE, a Prospective Multicenter Clinical Trial. Am J Respir Crit Care Med. 2021; 203:1306-1313. DOI

Affiliations

$authorString->getOrcid() =>

$authorString->getFullName() => Laura Melocchi

$authorString->getUrl() =>

Laura Melocchi

Fondazione Poliambulanza
non esiste orcidID ""

$authorString->getOrcid() =>

$authorString->getFullName() => Giulia Cervi

$authorString->getUrl() =>

Giulia Cervi

Respiratory Diseases Unit, Carlo Poma Hospital, Azienda Territoriale Socio Sanitaria (ATS) of Mantova, Mantova, Italy
non esiste orcidID ""

$authorString->getOrcid() =>

$authorString->getFullName() => Giuliana Sartori

$authorString->getUrl() =>

Giuliana Sartori

Operative Unit of Pathologic Anatomy, Azienda USL-IRCCS Reggio Emilia, Reggio Emilia, Italy
non esiste orcidID ""

$authorString->getOrcid() =>

$authorString->getFullName() => Laura Gandolfi

$authorString->getUrl() =>

Laura Gandolfi

Operative Unit of Pathology, Diagnostic Services Area, Fondazione Poliambulanza Hospital Institute, Brescia, Italy
non esiste orcidID ""

$authorString->getOrcid() =>

$authorString->getFullName() => Genny Jocollé

$authorString->getUrl() =>

Genny Jocollé

Operative Unit of Oncology, Azienda USL Valle d’Aosta, Aosta, Italy
non esiste orcidID ""

$authorString->getOrcid() =>

$authorString->getFullName() => Alberto Cavazza

$authorString->getUrl() =>

Alberto Cavazza

Operative Unit of Pathologic Anatomy, Azienda USL-IRCCS Reggio Emilia, Reggio Emilia, Italy
non esiste orcidID ""

$authorString->getOrcid() =>

$authorString->getFullName() => Giulio Rossi

$authorString->getUrl() =>

Giulio Rossi

Operative Unit of Pathology, Diagnostic Services Area, Fondazione Poliambulanza Hospital Institute, Brescia, Italy
non esiste orcidID ""

Copyright

© Società Italiana di Anatomia Patologica e Citopatologia Diagnostica, Divisione Italiana della International Academy of Pathology , 2023

How to Cite

[1]
Melocchi, L., Cervi, G., Sartori, G., Gandolfi, L., Jocollé, G., Cavazza, A. and Rossi, G. 2023. Up-regulation by overexpression of c-MET in fibroblastic foci of usual interstitial pneumonia. Pathologica - Journal of the Italian Society of Anatomic Pathology and Diagnostic Cytopathology. 115, 6 (Oct. 2023), 308-317.
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