Menin and p53 have non-synergistic effects on tumorigenesis in mice
- Kelly A Loffler†1Email author,
- Arne W Mould†1, 3,
- Paul M Waring2,
- Nicholas K Hayward1 and
- Graham F Kay1
© Loffler et al.; licensee BioMed Central Ltd. 2012
Received: 1 December 2011
Accepted: 18 June 2012
Published: 18 June 2012
While it is now more than a decade since the first description of the gene mutation underlying the tumour predisposition syndrome multiple endocrine neoplasia type 1 (MEN1), the mechanism by which its protein product menin acts to prevent development of tumours is still poorly understood.
We undertook a genetic experiment to assess whether menin synergises with p53. Mice carrying various combinations of Men1 and Trp53 mutations were generated then survival and pathology assessed.
While homozygous loss of Trp53 in mice resulted in early onset, aggressive tumours and profoundly reduced lifespan, heterozygous loss of either Trp53 or Men1 caused later onset disease, with a spectrum of tumours characteristic of each tumour suppressor gene. Loss of one copy of Men1 in animals also lacking both alleles of Trp53 did not exacerbate phenotype, based on survival, animal weight or sites of pathology, compared to Trp53 deletion alone. Dual heterozygous deletion of Men1 and Trp53 resulted in a small reduction in lifespan compared to the individual mutations, without new tumour sites. In the adrenal, we observed development of cortical tumours in dual heterozygous animals, as we have previously seen in Men1+/− animals, and there was loss of heterozygosity at the Men1 allele in these tumours. Median number of pathology observations per animal was increased in dual heterozygous animals compared with heterozygous loss of Trp53 alone.
Simultaneous heterozygous deletion of Men1 in animals with either heterozygous or homozygous deletion of Trp53 did not result in formation of tumours at any new sites, implying additive rather than synergistic effects of these pathways. Mice that were Men1+/− in addition to Trp53+/− had tumours in endocrine as well as other sites, implying that increase in total tumour burden, at sites typically associated with either Men1 or Trp53 loss, contributed to the slight decrease in survival in Men1+/−: Trp53+/− animals in comparison with their littermates.
Menin, the tumour suppressor product of the MEN1 gene that is mutated in the human tumour predisposition syndrome multiple endocrine neoplasia type 1 (MEN1), is a 610 amino acid protein with no homology to any known proteins [1, 2]. Menin localises predominantly to the nucleus, and is associated with a variety of proteins that implicate it in signal transduction pathways, as a transcriptional co-regulator, and in regulation of chromatin [3–5]. One of the proteins that associates with menin is the Fanconi anaemia protein FANCD2 , which is involved in response to DNA damage and participates in the BRCA/p53 pathway of tumour suppression .
Both spontaneous and familial cases of human MEN1 mutation result in predisposition to a range of tumour types, predominantly in endocrine organs such as parathyroid, pituitary and enteropancreatic sites . Several groups have published mouse models of MEN1, which replicate the human syndrome and result in tumour development, most commonly in endocrine pancreas, pituitary, parathyroid and thyroid glands, adrenals, in the gonads in some models, as well as other rarer sites [9–12].
Mutation of the TRP53 gene encoding p53 has been associated with many tumour types [for recent review of p53 biology see . Sporadic somatic mutations are commonly detected in different cancer types, and occur along the length of the gene. Hereditary TRP53 mutations are associated with Li Fraumeni syndrome (LFS), characterized by autosomal dominant inheritance and early onset tumour development, multiple tumours within an individual, and multiple affected family members. The most frequent tumour types in LFS are soft tissue sarcomas and osteosarcomas, breast cancer, brain tumours, leukaemia, and adrenocortical carcinoma (OMIM 151623). Mouse models of Trp53 deletion also exhibit a range of cancer types, particularly sarcoma and lymphoma [14, 15].
Our previous experiments have indicated that compound heterozygous loss of both Men1 and Rb1 genes has little effect on the rate, severity or onset of tumorigenesis, or on the spectrum of observed tumour types compared to individual gene deletions . In contrast, the comparable cross of animals with heterozygous loss of both Rb1 and Trp53 genes resulted in a marked increase in severity, decreased median lifespan, and the occurrence of novel tumour types not observed in either of the individual knockout animals [17, 18]. Trp53 can act synergistically with Brca2 and Cdkn2c, a known menin-regulated gene [5, 21]. p18, the protein product of Cdkn2c, also collaborates with menin to suppress neuroendocrine tumorigenesis . We therefore sought to ascertain whether a similar genetic interaction would be observed between Men1 and Trp53.
Mice with a targeted disruption of exon 2 of Men1 have been previously described, and were genotyped by PCR from tail or ear biopsy DNA . Mice with targeted deletion of Trp53 obtained from Tyler Jacks were maintained and genotyped as previously described . A cohort of animals including various combinations of the two tumour suppressor gene deletions were generated by cross-breeding and maintained under authorisation from the Queensland Institute of Medical Research Animal Ethics Committee in compliance with the Australian Code of Practice for the Care and Use of Animals for Scientific Purposes, in standard housing conditions with 12 hour light–dark cycle with food and water available ad libitum. Animals of the expected range of genotypes were born and viable, and all initially appeared normal and healthy. Cohorts were subsequently monitored periodically for signs of illness or overt tumour development. Upon observation of morbidity, animals were euthanased by CO2 asphyxiation, weighed, and a full necropsy carried out. At 21 months the experiment was terminated and all remaining animals culled and necropsies performed. At necropsy any pathology such as tumours or other grossly visible abnormalities were noted. Tissues were rinsed in PBS then fixed overnight in 10% neutral buffered formalin, washed in 70% ethanol and re-assessed using a stereomicroscope to confirm observations. Age was calculated using the date of birth and date of death to calculate the age in days, then dividing this value by 30.416667 to approximate the age in months. Survival was plotted in GraphPad Prism 5.01 for Windows, and Kaplan-Meier survival curves were analysed using Gehan-Breslow-Wilcoxon tests (GraphPad Software, San Diego U.S.A.). P values less than 0.05 were considered significant. Whole animal weights in grams were compared by one way ANOVA with Tukey’s correction for multiple comparisons. Pathology data from necropsy observations was tabulated by genotype group then analysed using PASW Statistics 17.0 (SPSS Inc., Chicago U.S.A.). Loss of heterozygosity was assessed by isolation of genomic DNA from formalin fixed tissues, followed by genotyping PCR as previously described . Products were separated by agarose gel electrophoresis, photographed and band intensities calculated using ImageJ image analysis software (NIH). Paraffin embedding and hematoxylin and eosin staining of tissues was carried out by the University of Queensland-Queensland Institute of Medical Research Histotechnology Facility, and sections were scanned using an Aperio Scanscope XT (Aperio Technologies, Vista U.S.A.). Histopathological assessment of adrenal sections was carried out a histopathologist (PMW), who was blinded to the genotypes of the animals.
Gross pathology observations
Pathology observed grossly, by anatomical site
1 L,1P/17 (5.9%L,5.9%P)
Pancreatic pathology observations
Adrenal pathology observations
Histological analysis revealed that large adrenal tumours in several Men1+/−: Trp53+/− animals were cortical adenomas or carcinomas, similar to those we had previously observed in our analysis of Men1+/− animals . Figure 3C shows adrenal histology from litter mate Men1+/−: Trp53+/+ and Men1+/−: Trp53+/− animals (14 and 12 months old respectively), in which both animals developed similar cortical adenoma and hyperplasia. In two Men1+/−: Trp53−/− animals in which pathology was grossly observed in the adrenal, histological assessment showed one of these to be a teratocarcinoma, and another was a poorly differentiated malignant neoplasm of uncertain origin, most likely an undifferentiated cortical carcinoma.
Occurrence of multiple pathology observations
Homozygous deletion of the mouse Men1 gene is lethal during embryogenesis [9, 23], while homozygous deletion of Trp53 in mice results in rapid onset development of multiple tumours and severely shortened lifespan compared to wild-type animals, or even to animals with heterozygous deletion of Trp53[14, 15]. Compound heterozygous Men1+/−: Trp53+/− animals described here were viable into adulthood, and median survival was much longer than the corresponding cohort of animals with homozygous deletion of Trp53, indicating that losing one copy each of both Men1 and Trp53 is not biologically equivalent to losing both copies of Trp53 or of Men1.
Animals with homozygous deletion of Trp53, particularly those which also had deletion of one copy of Men1, had lower whole body weights at necropsy, which we attribute primarily to the much younger age at which these animals showed onset of disease symptoms. A secondary contributing factor may be that when the Men1+/+: Trp53−/− and Men1+/−: Trp53−/− animals became ill they appeared to lose condition rapidly, and thus by the time of necropsy may have lost weight compared to remaining animals that were still healthy at the same age. This may be comparable to the wasting or cachexia often observed in human cancer patients.
We monitored the occurrence of tumours in these cohorts of animals and found that an endocrine pattern of tumorigenesis similar to that seen in MEN1 syndrome in humans, and in mice with heterozygous deletion of Men1, is still apparent when combined with heterozygous loss of p53. The tumour types associated with LFS in humans with heterozygous loss of TRP53 are not perfectly recapitulated by heterozygous or homozygous loss of Trp53 in mice, however each of these is associated with its own particular spectrum of tumour development [14, 15]. We have noted that each of these spectra is also retained in combination with Men1+/−. We thus conclude that mutations affecting either p53 or menin are associated with particular cellular consequences which correspond to propensity for tumorigenesis in particular tissues, and that additional mutations affecting the other pathway have negligible effect in terms of tissue specificity of tumour development. The absence of additional tumour sites is in contrast to previous descriptions of genetic interaction between Trp53 and Rb1 in which tumours develop in additional sites as well as with increased severity, resulting in dramatically shortened lifespan [17, 18].
Notably, the sites where pathology frequencies varied between Men1+/+: Trp53+/− and Men1+/−: Trp53+/− cohorts included the pancreas and pituitary, which are typical sites of Men1-associated tumorigenesis in mice, and the uterus, which may be affected by alterations in hormones secondary to pituitary pathology.
Both Li-Fraumeni and MEN1 syndromes are associated with high risk of development of multiple tumours (OMIM 151623 and 131100). This is also the case in both Men1+/− and Trp53+/− mice, as we and others have observed previously and confirmed here. The observation of highest median number of pathology observations per animal in the Men1+/−: Trp53+/− cohort indicates that tumours at more sites, likely corresponding to increased total tumour burden, was the cause underlying the steeper slope of the survival curve for these animals in comparison with either mutation alone. This resulted in the shortening of median lifespan for the Men1+/−: Trp53+/− cohort.
Mice with a combination of mutations affecting p53 and menin retain both of the tissue specific patterns of tumorigenesis associated with each of these tumour suppressors. They develop cancers in the endocrine pattern typically associated with MEN1 [8–12] and the sarcoma/lymphoma constellation that has been typically linked to the p53 pathway [14, 15]. These data imply that menin and p53 have independent and non-synergistic effects on tumorigenesis.
We cannot exclude the possibility that these mutations have consequences that result in changes in biology at a molecular level in individual cells, however this is not apparent at the level of gross tumour development. This implies some level of plasticity or compensation, or of independent pathways of activity for menin and p53.
We postulate that the increased total tumour burden, without new tumour types, in the compound Men1+/−: Trp53+/− cohort underlies the slightly shorter median survival of the compound heterozygous animals, compared to heterozygous loss of either of these tumour suppressor genes alone.
TRP53 is very frequently mutated in many types of tumours, however comprehensive sequencing of exomes of sporadic human pancreatic neurendocrine tumours identified mutations in Trp53 in only two of 68 tumours . The molecular pathway by which p53 acts to prevent tumour development can be disrupted in cancers by multiple mechanisms, not only by sequence mutation of the gene itself [for example  but the experiment described here provides genetic confirmation that disruption of the broader p53 pathway is unlikely to be important in these endocrine tumour types. Therapeutic avenues targeting the p53 pathway are therefore likely to be of little clinical utility in treatment of such tumours.
The authors acknowledge input from Dr. Magdalena Serewko-Auret, and the technical assistance of staff of the QIMR Small Animal Facility. NKH is a Senior Principal Research Fellow of the National Health and Medical Research Council of Australia. Work in NKH and GFK’s laboratories is supported by grants from the Australian Research Council, the National Health and Medical Research Council of Australia and the Cancer Council Queensland.
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