International Journal of Hematology

, Volume 97, Issue 1, pp 30–36 | Cite as

Ras/MAPK syndromes and childhood hemato-oncological diseases

Progress in Hematology Recent advances in genetic basis of childhood hemato-oncological diseases


Noonan syndrome (NS) is an autosomal-dominant disease characterized by distinctive facial features, webbed neck, cardiac anomalies, short stature and cryptorchidism. NS exhibits phenotypic overlap with Costello syndrome and cardio-facio-cutaneous (CFC) syndrome. Germline mutations of genes encoding proteins in the RAS/mitogen-activated protein kinase (MAPK) pathway cause NS and related disorders. Germline mutations in PTPN11, KRAS, SOS1, RAF1, and NRAS have been identified in 60–80 % of NS patients. Germline mutations in HRAS have been identified in patients with Costello syndrome and mutations in KRAS,BRAF, and MAP2K1/2 (MEK1/2) have been identified in patients with CFC syndrome. Recently, mutations in SHOC2 and CBL have been identified in patients with Noonan-like syndrome. It has been suggested that these syndromes be comprehensively termed RAS/MAPK syndromes, or RASopathies. Molecular analysis is beneficial for the confirmation of clinical diagnoses and follow-up with patients using a tumor-screening protocol, as patients with NS and related disorders have an increased risk of developing tumors. In this review, we summarize the genetic mutations, clinical manifestations, associations with malignant tumors, and possible therapeutic approaches for these disorders.


RAS/MAPK signaling pathway RASopathies Oncogene RAS RAF MEK 


Noonan syndrome (NS, MIM 163950) was first described by Jacqueline Noonan, a pediatric cardiologist, in 1962. NS is an autosomal dominant disorder characterized by short stature, facial dysmorphism and congenital heart defects. The distinctive facial features that manifest in NS include a webbed or short neck, hypertelorism, downslanting palpebral fissures, ptosis and low-set, posteriorly rotated ears [1, 2]. Congenital heart defects, including pulmonary valve stenosis, occur in 50–80 % of individuals. Hypertrophic cardiomyopathy is observed in 20 % of affected individuals. Other clinical manifestations include cryptorchidism, bleeding tendency, mild intellectual disability, deafness, and hydrops fetalis. The incidence of this syndrome is estimated to be between 1 in 1,000 and 1 in 2,500 live births [3]. NS is known to be associated with juvenile myelomonocytic leukemia (JMML), a myeloproliferative disorder characterized by excessive production of myelomonocytic cells [1].

The phenotypic features of NS are similar to those of Costello and cardio-facio-cutaneous (CFC) syndromes. Costello syndrome (MIM 218040) was originally described by Costello in 1971 [4] and explored further by the same author in 1977 [5]. Patients with Costello syndrome have distinctive facial characteristics, including full lips, a large mouth, and a full nasal tip, and exhibit mental retardation, high birth weight, neonatal feeding problems, curly hair, nasal papillomata, and soft skin with deep palmar and plantar creases [6]. Cardiac defects include hypertrophic cardiomyopathy, congenital heart defects and arrhythmia. Children and young adults with Costello syndrome have an increased risk of malignancy, which can be as high as approximately 17 % [7].

CFC syndrome (MIM 115150) was first described in 1986 [8], and the question of whether CFC and NS are distinct disorders or different phenotypes of the same condition is controversial. CFC syndrome is characterized by distinctive facial features, mental retardation, heart defects (pulmonic stenosis, atrial septal defect, and hypertrophic cardiomyopathy) and ectodermal abnormalities, such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition [9]. Typical facial characteristics include a high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge and posteriorly angulated ears with prominent helices.

NS with multiple lentigines was formerly referred to as LEOPARD syndrome. LEOPARD is an acronym for the cardinal features of the syndrome, which include multiple Lentigines, Electrocardiographic conduction abnormalities, Ocular hypertelorism, Pulmonary stenosis, Abnormal genitalia, Retardation of growth and sensorineural Deafness [10].

RAS GTPases are essential mediators in signaling pathways that convey extracellular stimuli from cell surface receptors to the cell. The Ras subfamily consists of classical Harvey-RAS (HRAS), Kirsten-RAS (KRAS) and neuroblastoma RAS (NRAS). Other distinct members include R-RAS, TC21 (R-RAS2), M-RAS (R-RAS3), Rap1A, Rap1B, Rap2A, Rap2B, RalA and RalB [11]. The RAS/mitogen-activated protein kinase (MAPK) pathway is an essential signaling pathway that controls cell proliferation, differentiation and survival. Recent studies have revealed that dysregulation of the RAS/MAPK pathway causes clinically overlapping genetic disorders, including NS, Costello syndrome, CFC syndrome, NS with multiple lentigines, neurofibromatosis type I, and Legius syndrome [6, 12]. This review outlines the molecular aspects, clinical manifestations, association with malignant tumors, and possible treatments of NS, Costello syndrome and CFC syndrome.

Genes and mutations that underlie genetic syndromes involving dysregulation of the RAS/MAPK signaling pathway (Table 1)


In 1994, linkage analysis of a large family with NS definitively established the first NS locus, which was defined as chromosomal bands 12q22-qter [13, 14]. In 2001, Tartaglia et al. [15] identified missense mutations in PTPN11, which encodes the tyrosine phosphatase SHP-2, in individuals with NS. Gain-of-function mutations in PTPN11 have been identified in approximately 50 % of individuals with clinically diagnosed NS [16, 17, 18] (Fig. 1). In contrast, loss-of-function or dominant negative mutations in PTPN11 have been reported in patients with NS with multiple lentigines [10]. In 2005, we performed candidate gene analysis of proteins in the RAS/MAPK cascade and discovered germline mutations in HRAS in patients with Costello syndrome [19]. Subsequently, mutations in KRAS, BRAF, and MAP2K1/2 have been identified in patients with CFC syndrome [20, 21], and mutations in KRAS, SOS1, RAF1, and NRAS have been identified in patients with NS [22, 23, 24, 25, 26, 27] (Fig. 1). Recently, mutations in SHOC2 [28] and CBL [29, 30, 31] have been identified in NS-like syndromes. These findings indicate that RAS and molecules downstream of RAS play essential roles in human development. It has been suggested that these syndromes be comprehensively termed ‘RAS/MAPK syndromes’ or ‘RASopathies’ [6, 12].
Table 1

Summary of RAS/MAPK syndromes




Gene(s) mutated





Noonan-like disorder with loose anagen hair




NS-like disorder




Costello syndrome




Cardio-facio-cutaneous (CFC) syndrome




Neurofibromatosis type I




NF-1 like syndrome (Legius syndrome)




NS with multiple lentigines (LEOPARD syndrome)




Hereditary gingival fibromatosis




Capillary malformation-arteriovenous malformation




MIM Mendelian inheritance in man, AD autosomal dominant, LEOPARD multiple Lentigines, Electrocardiographic conduction abnormalities, Ocular hypertelorism, Pulmonary stenosis, Abnormal genitalia, Retardation of growth and sensorineural Deafness

Fig. 1

RAS/MAPK cascade and disorders involving germline mutations of related genes

Genes and mutations


SHP-2, the product of PTPN11, is a widely expressed cytoplasmic tyrosine phosphatase that has been implicated in signal transduction pathways elicited by growth factors, cytokines, hormones and the extracellular matrix [32]. SHP-2 comprises a tandem array of two SH2 domains at its N-terminus, a catalytic domain in the middle, and a C-terminal domain that contains tyrosine phosphorylation sites. Most mutations identified in NS were clustered in exons 3, 4, 7, 8, 12 and 13. Y63C, Q79R, N308D, and N308S were the most common mutations [6, 33]. T73I has been frequently identified in NS patients with JMML. Specific mutations (Y279C, A461T, G464A, T468M, D498W and Q510P) have been identified in NS with multiple lentigines.

Mutations that have been previously identified in NS are located in the interacting face of the N-SH2 domain and phosphatase domain, suggesting that they are gain-of-function mutations that enhance phosphatase activity. SHP-2 mutants associated with leukemia were more catalytically active than mutants identified in NS patients, suggesting that a high level of SHP-2 activation is associated with neoplastic diseases, whereas a lower level of SHP-2 activation causes NS [17, 34, 35, 36]. Mutations identified in NS with multiple lentigines have been shown to be catalytically inactive or dominant negative [36, 37, 38].


SOS1 is a ubiquitously expressed guanine nucleotide exchange factor (GEF) that is responsible for the activation of RAS proteins by catalyzing GDP/GTP exchange. Mutations in SOS1 have been identified in 8–14 % of patients with NS [25, 27], and the biochemical characterization of SOS1 mutants has indicated enhanced protein function and increased downstream signaling. Compared with other NS patients, the incidence of short stature and intellectual disability is lower in patients who tested positive for an SOS1 mutation [39].


RAF1 is a member of the RAS serine–threonine kinase family. Mutations in RAF1 have been identified in 3–17 % of patients with NS and a small number of patients with NS with multiple lentigines [23, 24]. Mutations identified in NS were clustered in conserved region (CR) 2, which contains an inhibitory phosphorylation site (serine at position 259; S259). RAF1 mutations located in the CR2 domain caused a decrease in the phosphorylation of S259, leading to partial ERK activation [39]. Notably, 70 % of patients with RAF1 mutations exhibit hypertrophic cardiomyopathy [23, 24, 39, 40].


Individuals with HRAS mutations are diagnosed as having Costello syndrome, and heterozygous HRAS mutations have been identified in more than 90 % of patients with this syndrome [6, 19]. Germline mutations are clustered in codons 12 and 13, and the G12S mutation is the most frequent (80 %). HRAS germline mutations occur de novo. Somatic mosaicism for the G12S mutation has been reported in three individuals with clinical findings suggestive for Costello syndrome [41].


Individuals with KRAS mutations exhibit variable phenotypes and are diagnosed with NS or CFC syndrome [20, 26, 42]. Mutations in codons 12, 13, and 61, which are frequent in somatic cancers, have rarely been identified as germline mutations, which is in contrast with HRAS germline mutations. V14I is a frequent mutation in NS, and D153V mutation has been identified in patients with NS or CFC syndrome [6]. The effects of KRAS germline mutations on the downstream pathway are less pronounced than the effects of somatic mutations [20, 26]

BRAF and MAP2K1/2 (MEK1/2)

Mutations in BRAF and MAP2K1/2 have been identified in patients with CFC syndrome [20, 21]. BRAF mutations have also been identified in patients with a phenotype of NS with multiple lentigines. Somatic mutations in BRAF have been identified in 7 % of all cancers, including human malignant melanoma and colorectal cancer [43]. V600E mutation in the activation segment in the kinase domain (CR3) has been frequently identified in somatic cancers (>90 %). Germline mutations were clustered in the cysteine-rich domain (CR1 domain) and kinase domain. The distribution of the mutations identified in CFC syndrome partially overlapped with that of the mutations identified in cancers. Q257R and E501G are frequent mutations in CFC syndrome [6]. Germline mutations in MAP2K1/2 are clustered in exons 2 and 3. ERK phosphorylation was enhanced in cells transfected with mutant MEK1 or MEK2 [21]. Affected individuals harboring BRAF and MAP2K1/2 mutations have the disorder as a result of a de novo mutation. One family transmitting an autosomal dominant germline mutation in MAP2K2 has been reported [44].


SHOC2 is homologous to soc2, a gene discovered in Caenorhabditis elegans. The soc2 gene encodes leucine-rich repeats [45] and acts as a positive modulator of the RAS/MAPK pathway [46]. In 2009, a gain-of-function missense mutation in SHOC2, c.4A > G (p.S2G), was identified in patients with Noonan-like syndrome with loose anagen hair [28]. The clinical features associated with the S2G mutation are distinct from those associated with NS and include a high frequency of loose anagen hair, more severe intellectual disabilities, skin abnormalities, and a hypernasal voice [28, 47]. Wild-type SHOC2 is localized in the nucleus and cytoplasm, while the mutant protein (S2G) promoted aberrant N-myristoylation, localized to the plasma membrane and resulted in ERK activation [28].


A germline mutation in NRAS has been reported in a patient with autoimmune lymphoproliferative syndrome. Germline mutations in NRAS have been reported in four of 917 NS patients (0.4 %) who were negative for previously known mutations [22]. The amino acid changes identified in NS patients were I24N, P34L, T50I and G60E [22, 48, 49]. Cells carrying T50I and G60E mutations and oncogenic G12V displayed enhanced MEK and ERK phosphorylation when serum was added to the growth medium [22].


Casitas B-cell lymphoma (CBL) is the cellular homolog of the v-Cbl transforming gene of the Cas NS-1 murine leukemia virus. CBL functions primarily as an E3 ubiquitin ligase and is responsible for the intracellular transport and degradation of a large number of proteins. The majority of CBL somatic mutations have been reported in myelodysplastic syndromes/myeloproliferative disorders, including chronic myelomonocytic, juvenile myelomonocytic and atypical chronic myeloid leukemias. Germline mutations in CBL have been identified in JMML patients who displayed a variable combination of dysmorphic features reminiscent of the facial gestalt of NS [29, 30, 31].

Association of tumors and hematologic malignancies in patients with germline mutations in genes within the RAS/MAPK pathway (Table 2)

Somatic mutations in genes in the RAS pathway, including PTPN11, HRAS, KRAS, NRAS, BRAF and CBL, have been identified in a variety of solid tumors and hematologic malignancies. NS and related disorders are known to cause a predisposition to cancer. The precise frequency of tumor predisposition in mutation-positive patients remains unknown.
Table 2

Disorders involving germline and somatic mutations in genes of the RAS/MAPK cascade


Germline mutations

Somatic mutations


Associated tumors

Tumors and related disorders


NS, NS with multiple lentigines (LEOPARD syndrome)

JMML, myeloproliferative disorders [50]

JMML, AML, ALL, MDS, CML, solid tumors



Rhabdomyosarcoma (1 pt), Sertoli cell tumor (1 pt), granular cell tumors (1 pt) [55]

Rare (astrocytoma, lung cancer)


NS, NS with multiple lentigines (LEOPARD syndrome)

Rare (AML, lung cancer, ovarian cancer, colon cancer)


Noonan-like disorder with loose anagen hair



Hematologic malignancies


NS-like disorder

JMML [30, 31]

JMML, CML, AML, MDS, lung cancer


Costello syndrome

Rhabdomyosarcoma, neuroblastoma, bladder carcinoma, papillomata

Bladder carcinoma


CFC syndrome, NS

JMML (1 pt) [26]

Pancreatic tumor, colon cancer, lung cancer, RAS-associated ALPS-like disease [63]


CFC syndrome NS

ALL (2 pts) [20, 51], non-Hodgkin lymphoma (1 pt) [52]

Malignant melanoma, colon cancer, thyroid cancer, Langerhans cell histiocytosis [53]


CFC syndrome

Hepatoblastoma (1 pt) [54]


CFC syndrome

JMML juvenile myelomonocytic leukemia, ALL acute lymphoblastic leukemia, AML acute myelogenous leukemia, CML chronic myelogenous leukemia, MDS myelodysplastic syndromes, ALPS autoimmune lymphoproliferative syndrome

It has been reported that the PTPN11 mutations in patients with NS are frequently associated with hematologic malignancies, including acute lymphoblastic leukemia and JMML. The frequency of association with tumors remains unknown. In a summary of the literature, Kratz et al. [50] reported that 45 of 1,151 patients (3.9 %) with NS (mutation status unknown) developed cancer; of these, eight patients presented with neuroblastoma, and eight presented with acute lymphoblastic leukemia. The other cancers identified included six gliomas, six rhabdomyosarcoma, three acute myeloid leukemias, three testicular cancers, two non-Hodgkin lymphomas and two colon cancers. PTPN11 mutations in patients with NS have been shown to be associated with myeloproliferative disorder, and with a benign course in 40 % of such patients, and an aggressive course in 15 % [50]. It remains unknown why gain-of-function mutations in PTPN11 enhance the proliferation of specific lineages in hematologic malignancies.

Approximately, 10–15 % of patients with Costello syndrome develop malignant tumors, including rhabdomyosarcoma, neuroblastoma (in infants) and transitional cell carcinoma of the bladder (in adolescents and young adults) [6]. A tumor screening protocol for patients with Costello syndrome has been proposed [7]. Notably, HRAS mutations were originally identified in bladder carcinoma cell lines. It remains unknown why patients with HRAS germline mutations develop bladder carcinomas.

Little attention had been given to the development of tumors in patients with CFC syndrome until molecular analysis became available. Two CFC patients with BRAF mutations were reported to have developed acute lymphoblastic leukemia [20, 51], and one CFC patient with a BRAF mutation was reported to have developed non-Hodgkin lymphoma [52]. Somatic BRAF mutations in hematologic malignancies do not occur frequently, but they are substantially reported. Recently, BRAF mutations have been identified in Langerhans cell histiocytosis [53]. It is possible that the role of BRAF in hematologic malignancies may indicate that BRAF plays roles in other malignancies beyond solid tumors. As for MAP2K1/2, one patient with a MAP2K1 mutation developed hepatoblastoma [54].

Germline mutations in CBL have been identified in JMML patients who displayed a variable combination of dysmorphic features reminiscent of the facial gestalt of NS. Facial appearances, psychomotor development, head circumference and skin abnormalities should be carefully observed in children with hematologic malignancies. A patient with a KRAS mutation who developed JMML has been reported [26]. It has been reported that three patients with SOS1 germline mutations developed rhabdomyosarcoma (one patient), Sertoli cell tumors (one patient), and granular cell tumors (one patient) [55]. As far as we know, tumor association has not been reported in individuals with germline mutations in SHOC2, NRAS, and RAF1.

The natural history and predisposition for hematologic malignancies and solid tumors in adults with RAS/MAPK syndromes have not been clarified. We conducted a nationwide epidemiologic study on patients with Costello and CFC syndromes in 2009 [56]. The results showed that the total number of patients with Costello and CFC syndrome in Japan was estimated to be 99 (95 % confidence interval, 77–120) and 157 (95 % confidence interval, 86–229), respectively. An evaluation of 15 adult patients (18–32 years of age) revealed that one had recurrent bladder papillomata and another had multiple gallbladder polyps and a renal angioma. None of the examined patients developed malignant tumors. Twelve of 15 adult patients had moderate to severe mental retardation, but eleven live at home, and 10 can walk independently, suggesting that a portion of adult patients may be unrecognized and the number of adult patients is likely underestimated. Therefore, the prognosis, including the frequency of malignant tumors, remains to be elucidated in adults with germline mutations in RAS and RAF.


The identification of the causative genes underlying NS and related disorders has facilitated the molecular diagnosis of these disorders, allowed the evaluation of the genotype–phenotype relationship and helped develop possible therapeutic approaches. In approximately 10–30 % of patients with RAS/MAPK syndromes, no mutations were identified. The introduction of exome sequencing will lead to the identification of novel genes involved in these disorders.

The regulation and inhibition of the RAS/MAPK pathway have been well studied in cancer research. Inhibitors of the RAS/MAPK cascade may provide opportunities to therapeutically treat disorders involving dysregulation of the RAS/MAPK pathway [57]. Indeed, MEK inhibitors ameliorated the phenotype of mice models for NS (mutations in SOS1 and RAF1) [58, 59] and Costello syndrome (mutation in HRAS) [60]. An inhibitor of mTOR has been shown to reverse heart defects in a mouse model for NS with multiple lentigines [61]. HMG-CoA reductase inhibitors have been used in clinical trials to treat cognitive function in individuals with NF1 [62]. These results suggest that the phenotypes in RAS/MAPK syndromes can be ameliorated by the manipulation of RAS/MAPK activity.


  1. 1.
    van der Burgt I. Noonan syndrome. Orphanet J Rare Dis. 2007;2:4.PubMedCrossRefGoogle Scholar
  2. 2.
    Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, et al. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010;126:746–59.PubMedCrossRefGoogle Scholar
  3. 3.
    Allanson JE, Hall JG, Hughes HE, Preus M, Witt RD. Noonan syndrome: the changing phenotype. Am J Med Genet. 1985;21:507–14.PubMedCrossRefGoogle Scholar
  4. 4.
    Costello J. A new syndrome. N Z Med J. 1971;74:397.Google Scholar
  5. 5.
    Costello JM. A new syndrome: mental subnormality and nasal papillomata. Aust Paediatr J. 1977;13:114–8.PubMedGoogle Scholar
  6. 6.
    Aoki Y, Niihori T, Narumi Y, Kure S, Matsubara Y. The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders. Hum Mutat. 2008;29:992–1006.PubMedCrossRefGoogle Scholar
  7. 7.
    Gripp KW, Scott CI Jr, Nicholson L, McDonald-McGinn DM, Ozeran JD, Jones MC, et al. Five additional Costello syndrome patients with rhabdomyosarcoma: proposal for a tumor screening protocol. Am J Med Genet. 2002;108:80–7.PubMedCrossRefGoogle Scholar
  8. 8.
    Reynolds JF, Neri G, Herrmann JP, Blumberg B, Coldwell JG, Miles PV, et al. New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement—the CFC syndrome. Am J Med Genet. 1986;25:413–27.PubMedCrossRefGoogle Scholar
  9. 9.
    Allanson JE, Anneren G, Aoki Y, Armour CM, Bondeson ML, Cave H, et al. Cardio-facio-cutaneous syndrome: does genotype predict phenotype? Am J Med Genet C Semin Med Genet. 2011;157:129–35.PubMedCrossRefGoogle Scholar
  10. 10.
    Digilio MC, Conti E, Sarkozy A, Mingarelli R, Dottorini T, Marino B, et al. Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene. Am J Hum Genet. 2002;71:389–94.PubMedCrossRefGoogle Scholar
  11. 11.
    Takai Y, Sasaki T, Matozaki T. Small GTP-binding proteins. Physiol Rev. 2001;81:153–208.PubMedGoogle Scholar
  12. 12.
    Tidyman WE, Rauen KA. The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation. Curr Opin Genet Dev. 2009;19:230–6.PubMedCrossRefGoogle Scholar
  13. 13.
    Jamieson CR, van der Burgt I, Brady AF, van Reen M, Elsawi MM, Hol F, et al. Mapping a gene for Noonan syndrome to the long arm of chromosome 12. Nat Genet. 1994;8:357–60.PubMedCrossRefGoogle Scholar
  14. 14.
    van der Burgt I, Berends E, Lommen E, van Beersum S, Hamel B, Mariman E. Clinical and molecular studies in a large Dutch family with Noonan syndrome. Am J Med Genet. 1994;53:187–91.PubMedCrossRefGoogle Scholar
  15. 15.
    Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H, et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet. 2001;29:465–8.PubMedCrossRefGoogle Scholar
  16. 16.
    Musante L, Kehl HG, Majewski F, Meinecke P, Schweiger S, Gillessen-Kaesbach G, et al. Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome. Eur J Hum Genet. 2003;11:201–6.PubMedCrossRefGoogle Scholar
  17. 17.
    Niihori T, Aoki Y, Ohashi H, Kurosawa K, Kondoh T, Ishikiriyama S, et al. Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. J Hum Genet. 2005;50:192–202.PubMedCrossRefGoogle Scholar
  18. 18.
    Tartaglia M, Kalidas K, Shaw A, Song X, Musat DL, van der Burgt I, et al. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet. 2002;70:1555–63.PubMedCrossRefGoogle Scholar
  19. 19.
    Aoki Y, Niihori T, Kawame H, Kurosawa K, Ohashi H, Tanaka Y, et al. Germline mutations in HRAS proto-oncogene cause Costello syndrome. Nat Genet. 2005;37:1038–40.PubMedCrossRefGoogle Scholar
  20. 20.
    Niihori T, Aoki Y, Narumi Y, Neri G, Cave H, Verloes A, et al. Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome. Nat Genet. 2006;38:294–6.PubMedCrossRefGoogle Scholar
  21. 21.
    Rodriguez-Viciana P, Tetsu O, Tidyman WE, Estep AL, Conger BA, Cruz MS, et al. Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome. Science. 2006;311:1287–90.PubMedCrossRefGoogle Scholar
  22. 22.
    Cirstea IC, Kutsche K, Dvorsky R, Gremer L, Carta C, Horn D, et al. A restricted spectrum of NRAS mutations causes Noonan syndrome. Nat Genet. 2010;42:27–9.PubMedCrossRefGoogle Scholar
  23. 23.
    Pandit B, Sarkozy A, Pennacchio LA, Carta C, Oishi K, Martinelli S, et al. Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. Nat Genet. 2007;39:1007–12.PubMedCrossRefGoogle Scholar
  24. 24.
    Razzaque MA, Nishizawa T, Komoike Y, Yagi H, Furutani M, Amo R, et al. Germline gain-of-function mutations in RAF1 cause Noonan syndrome. Nat Genet. 2007;39:1013–7.PubMedCrossRefGoogle Scholar
  25. 25.
    Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, et al. Germline gain-of-function mutations in SOS1 cause Noonan syndrome. Nat Genet. 2007;39:70–4.PubMedCrossRefGoogle Scholar
  26. 26.
    Schubbert S, Zenker M, Rowe SL, Boll S, Klein C, Bollag G, et al. Germline KRAS mutations cause Noonan syndrome. Nat Genet. 2006;38:331–6.PubMedCrossRefGoogle Scholar
  27. 27.
    Tartaglia M, Pennacchio LA, Zhao C, Yadav KK, Fodale V, Sarkozy A, et al. Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. Nat Genet. 2007;39:75–9.PubMedCrossRefGoogle Scholar
  28. 28.
    Cordeddu V, Di Schiavi E, Pennacchio LA, Ma’ayan A, Sarkozy A, Fodale V, et al. Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair. Nat Genet. 2009;41:1022–6.PubMedCrossRefGoogle Scholar
  29. 29.
    Martinelli S, De Luca A, Stellacci E, Rossi C, Checquolo S, Lepri F, et al. Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. Am J Hum Genet. 2010;87:250–7.PubMedCrossRefGoogle Scholar
  30. 30.
    Niemeyer CM, Kang MW, Shin DH, Furlan I, Erlacher M, Bunin NJ, et al. Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia. Nat Genet. 2010;42:794–800.PubMedCrossRefGoogle Scholar
  31. 31.
    Perez B, Mechinaud F, Galambrun C, Ben Romdhane N, Isidor B, Philip N, et al. Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia. J Med Genet. 2010;47:686–91.PubMedCrossRefGoogle Scholar
  32. 32.
    Neel BG, Gu H, Pao L. The ‘Shp’ing news: SH2 domain-containing tyrosine phosphatases in cell signaling. Trends Biochem Sci. 2003;28:284–93.PubMedCrossRefGoogle Scholar
  33. 33.
    Tartaglia M, Gelb BD. Germ-line and somatic PTPN11 mutations in human disease. Eur J Med Genet. 2005;48:81–96.PubMedCrossRefGoogle Scholar
  34. 34.
    Fragale A, Tartaglia M, Wu J, Gelb BD. Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activation. Hum Mutat. 2004;23:267–77.PubMedCrossRefGoogle Scholar
  35. 35.
    Keilhack H, David FS, McGregor M, Cantley LC, Neel BG. Diverse biochemical properties of Shp2 mutants. Implications for disease phenotypes. J Biol Chem. 2005;280:30984–93.PubMedCrossRefGoogle Scholar
  36. 36.
    Tartaglia M, Martinelli S, Stella L, Bocchinfuso G, Flex E, Cordeddu V, et al. Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease. Am J Hum Genet. 2006;78:279–90.PubMedCrossRefGoogle Scholar
  37. 37.
    Hanna N, Montagner A, Lee WH, Miteva M, Vidal M, Vidaud M, et al. Reduced phosphatase activity of SHP-2 in LEOPARD syndrome: consequences for PI3K binding on Gab1. FEBS Lett. 2006;580:2477–82.PubMedCrossRefGoogle Scholar
  38. 38.
    Kontaridis MI, Swanson KD, David FS, Barford D, Neel BG. PTPN11 (Shp2) mutations in LEOPARD syndrome have dominant negative, not activating, effects. J Biol Chem. 2006;281:6785–92.PubMedCrossRefGoogle Scholar
  39. 39.
    Kobayashi T, Aoki Y, Niihori T, Cave H, Verloes A, Okamoto N, et al. Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation. Hum Mutat. 2010;31:284–94.PubMedCrossRefGoogle Scholar
  40. 40.
    Ko JM, Kim JM, Kim GH, Yoo HW. PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome. J Hum Genet. 2008;53:999–1006.PubMedCrossRefGoogle Scholar
  41. 41.
    Girisha KM, Lewis LE, Phadke SR, Kutsche K. Costello syndrome with severe cutis laxa and mosaic HRAS G12S mutation. Am J Med Genet A. 2010;152A:2861–4.PubMedCrossRefGoogle Scholar
  42. 42.
    Zenker M, Lehmann K, Schulz AL, Barth H, Hansmann D, Koenig R, et al. Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations. J Med Genet. 2007;44:131–5.PubMedCrossRefGoogle Scholar
  43. 43.
    Garnett MJ, Marais R. Guilty as charged: B-RAF is a human oncogene. Cancer Cell. 2004;6:313–9.PubMedCrossRefGoogle Scholar
  44. 44.
    Rauen KA, Tidyman WE, Estep AL, Sampath S, Peltier HM, Bale SJ, et al. Molecular and functional analysis of a novel MEK2 mutation in cardio-facio-cutaneous syndrome: transmission through four generations. Am J Med Genet A. 2010;152A:807–14.PubMedCrossRefGoogle Scholar
  45. 45.
    Selfors LM, Schutzman JL, Borland CZ, Stern MJ. soc-2 encodes a leucine-rich repeat protein implicated in fibroblast growth factor receptor signaling. Proc Natl Acad Sci USA. 1998;95:6903–8.PubMedCrossRefGoogle Scholar
  46. 46.
    Rodriguez-Viciana P, Oses-Prieto J, Burlingame A, Fried M, McCormick F. A phosphatase holoenzyme comprised of Shoc2/Sur8 and the catalytic subunit of PP1 functions as an M-Ras effector to modulate Raf activity. Mol Cell. 2006;22:217–30.PubMedCrossRefGoogle Scholar
  47. 47.
    Komatsuzaki S, Aoki Y, Niihori T, Okamoto N, Hennekam RC, Hopman S, et al. Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies. J Hum Genet. 2010;55:801–9.PubMedCrossRefGoogle Scholar
  48. 48.
    Denayer E, Peeters H, Sevenants L, Derbent M, Fryns JP, Legius E. NRAS mutations in Noonan syndrome. Mol Syndromol. 2012;3:34–8.PubMedGoogle Scholar
  49. 49.
    Runtuwene V, van Eekelen M, Overvoorde J, Rehmann H, Yntema HG, Nillesen WM, et al. Noonan syndrome gain-of-function mutations in NRAS cause zebrafish gastrulation defects. Dis Model Mech. 2011;4:393–9.PubMedCrossRefGoogle Scholar
  50. 50.
    Kratz CP, Rapisuwon S, Reed H, Hasle H, Rosenberg PS. Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes. Am J Med Genet C Semin Med Genet. 2011;157:83–9.PubMedCrossRefGoogle Scholar
  51. 51.
    Makita Y, Narumi Y, Yoshida M, Niihori T, Kure S, Fujieda K, et al. Leukemia in Cardio-facio-cutaneous (CFC) syndrome: a patient with a germline mutation in BRAF proto-oncogene. J Pediatr Hematol Oncol. 2007;29:287–90.PubMedCrossRefGoogle Scholar
  52. 52.
    Ohtake A, Aoki Y, Saito Y, Niihori T, Shibuya A, Kure S, et al. Non-hodgkin lymphoma in a patient with cardiofaciocutaneous syndrome. J Pediatr Hematol Oncol. 2011;33:e342–6.PubMedCrossRefGoogle Scholar
  53. 53.
    Badalian-Very G, Vergilio JA, Degar BA, MacConaill LE, Brandner B, Calicchio ML, et al. Recurrent BRAF mutations in Langerhans cell histiocytosis. Blood. 2010;116:1919–23.PubMedCrossRefGoogle Scholar
  54. 54.
    Al-Rahawan MM, Chute DJ, Sol-Church K, Gripp KW, Stabley DL, McDaniel NL, et al. Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndrome. Am J Med Genet A. 2007;143A:1481–8.PubMedCrossRefGoogle Scholar
  55. 55.
    Denayer E, Devriendt K, de Ravel T, Van Buggenhout G, Smeets E, Francois I, et al. Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations. Genes Chromosomes Cancer. 2010;49:242–52.PubMedGoogle Scholar
  56. 56.
    Abe Y, Aoki Y, Kuriyama S, Kawame H, Okamoto N, Kurosawa K, et al. Prevalence and clinical features of Costello syndrome and cardio-facio-cutaneous syndrome in Japan: findings from a nationwide epidemiological survey. Am J Med Genet A. 2012;158A:1083–94.PubMedCrossRefGoogle Scholar
  57. 57.
    Rauen KA, Banerjee A, Bishop WR, Lauchle JO, McCormick F, McMahon M, et al. Costello and cardio-facio-cutaneous syndromes: moving toward clinical trials in RASopathies. Am J Med Genet C Semin Med Genet. 2011;157:136–46.PubMedCrossRefGoogle Scholar
  58. 58.
    Chen PC, Wakimoto H, Conner D, Araki T, Yuan T, Roberts A, et al. Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome-associated Sos1 mutation. J Clin Invest. 2010;120:4353–65.PubMedCrossRefGoogle Scholar
  59. 59.
    Wu X, Simpson J, Hong JH, Kim KH, Thavarajah NK, Backx PH, et al. MEK–ERK pathway modulation ameliorates disease phenotypes in a mouse model of Noonan syndrome associated with the Raf1(L613V) mutation. J Clin Invest. 2011;121:1009–25.PubMedCrossRefGoogle Scholar
  60. 60.
    Schuhmacher AJ, Guerra C, Sauzeau V, Canamero M, Bustelo XR, Barbacid M. A mouse model for Costello syndrome reveals an Ang II-mediated hypertensive condition. J Clin Invest. 2008;118:2169–79.PubMedGoogle Scholar
  61. 61.
    Marin TM, Keith K, Davies B, Conner DA, Guha P, Kalaitzidis D, et al. Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome-associated PTPN11 mutation. J Clin Invest. 2011;121:1026–43.PubMedCrossRefGoogle Scholar
  62. 62.
    Krab LC, de Goede-Bolder A, Aarsen FK, Pluijm SM, Bouman MJ, van der Geest JN, et al. Effect of simvastatin on cognitive functioning in children with neurofibromatosis type 1: a randomized controlled trial. JAMA. 2008;300:287–94.PubMedCrossRefGoogle Scholar
  63. 63.
    Takagi M, Shinoda K, Piao J, Mitsuiki N, Matsuda K, Muramatsu H, et al. Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation. Blood. 2011;117:2887–90.Google Scholar

Copyright information

© The Japanese Society of Hematology 2012

Authors and Affiliations

  1. 1.Department of Medical GeneticsTohoku University School of MedicineSendaiJapan

Personalised recommendations