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29 Results Found

  • Case Report
  • Open Access
5 Citations
2,297 Views
7 Pages

Interhemispheric Pediatric Meningioma, YAP1 Fusion-Positive

  • Silvia Esposito,
  • Gianluca Marucci,
  • Manila Antonelli,
  • Evelina Miele,
  • Piergiorgio Modena,
  • Marzia Giagnacovo,
  • Maura Massimino,
  • Veronica Biassoni,
  • Matilde Taddei and
  • Marco Paolo Schiariti
  • + 4 authors

29 September 2022

Meningiomas are uncommon in children and usually arise in the context of tumor-predisposing syndromes. Recently, YAP1-fusions have been identified for the first time as potential NF2-independent oncogenic drivers in the development of meningiomas in...

  • Case Report
  • Open Access
7 Citations
2,253 Views
6 Pages

15 August 2023

Oncogenic Yes-associated protein (YAP) 1 fusions have been recently identified in several cases of meningioma mostly involving pediatric patients. The meningiomas harboring YAP1-MAML2, which is the most frequent fusion subtype, exhibit activated YAP1...

  • Feature Paper
  • Review
  • Open Access
44 Citations
9,158 Views
16 Pages

10 July 2018

Epithelioid hemangioendothelioma (EHE) is a rare soft-tissue sarcoma involving cells with histologic markers that suggest an endothelial origin. Around 90% of EHEs are caused by the fusion of Transcriptional Co-activator with a PDZ-motif (TAZ) with C...

  • Article
  • Open Access
7 Citations
3,308 Views
17 Pages

JTE-013 Alleviates Pulmonary Fibrosis by Affecting the RhoA/YAP Pathway and Mitochondrial Fusion/Fission

  • Jiaxu Zhou,
  • Yilan Song,
  • Xingmei Wang,
  • Xinrui Li,
  • Chang Liu,
  • Chenchen Tian,
  • Chongyang Wang,
  • Liangchang Li,
  • Guanghai Yan and
  • Hong Cui

12 October 2023

Pulmonary fibrosis may be due to the proliferation of fibroblasts and the aggregation of extracellular matrix, resulting in the stimulation of inflammation damage, destroying lung tissue structure, seriously affecting the patient’s respiratory...

  • Article
  • Open Access
4 Citations
3,520 Views
20 Pages

A Matched Molecular and Clinical Analysis of the Epithelioid Haemangioendothelioma Cohort in the Stafford Fox Rare Cancer Program and Contextual Literature Review

  • Arwa Abdelmogod,
  • Lia Papadopoulos,
  • Stephen Riordan,
  • Melvin Wong,
  • Martin Weltman,
  • Ratana Lim,
  • Christopher McEvoy,
  • Andrew Fellowes,
  • Stephen Fox and
  • Justin Bedő
  • + 16 authors

1 September 2023

Background: Epithelioid haemangioendothelioma (EHE) is an ultra-rare malignant vascular tumour with a prevalence of 1 per 1,000,000. It is typically molecularly characterised by a WWTR1::CAMTA1 gene fusion in approximately 90% of cases, or a YAP1::TF...

  • Review
  • Open Access
8 Citations
3,293 Views
30 Pages

Genetic Alterations and Deregulation of Hippo Pathway as a Pathogenetic Mechanism in Bone and Soft Tissue Sarcoma

  • Carmen Salguero-Aranda,
  • Joaquín Olmedo-Pelayo,
  • Enrique de Álava,
  • Ana Teresa Amaral and
  • Juan Díaz-Martín

15 December 2022

The Hippo pathway is an evolutionarily conserved modulator of developmental biology with a key role in tissue and organ size regulation under homeostatic conditions. Like other signaling pathways with a significant role in embryonic development, the...

  • Review
  • Open Access
1,953 Views
20 Pages

The Current Landscape of Molecular Pathology for the Diagnosis and Treatment of Ependymoma

  • Alyssa Steller,
  • Ashley Childress,
  • Alayna Koch,
  • Emma Vallee and
  • Scott Raskin

4 September 2025

Ependymomas are a heterogeneous group of central nervous system tumors originating from ependymal cells, exhibiting significant variability in clinical behavior, prognosis, and treatment response based on anatomical location and molecular profile. Hi...

  • Review
  • Open Access
15 Citations
5,064 Views
16 Pages

16 June 2022

The activities of YAP and TAZ, the end effectors of the Hippo pathway, are consistently altered in cancer, and this dysregulation drives aggressive tumor phenotypes. While the actions of these two proteins aid in tumorigenesis in the majority of canc...

  • Review
  • Open Access
33 Citations
7,173 Views
13 Pages

Diagnosis and Management of Porocarcinoma

  • Kodai Miyamoto,
  • Teruki Yanagi,
  • Takuya Maeda and
  • Hideyuki Ujiie

25 October 2022

Eccrine porocarcinoma, also known as porocarcinoma (PC) and malignant eccrine poroma, is very rare and is known to arise from the cutaneous intraepidermal ducts of the sweat glands. Its etiology is not well understood; however, some studies suggest t...

  • Article
  • Open Access
14 Citations
3,408 Views
20 Pages

9 September 2021

Maintenance of redox homeostasis is vital for aerobic organisms and particularly relevant to plant pathogens. A balance is required between their endogenous ROS production, which is important for their development and pathogenicity, and host-derived...

  • Article
  • Open Access
1 Citations
3,029 Views
12 Pages

Effect of Prooxidative Natural Products: Comparison of the OSI1 (YKL071w) Promoter Luciferase Construct from Yeast with an Nrf2/Keap Reporter System

  • Ivan Schlembach,
  • Andreas Uebachs,
  • Tim Caspers,
  • Athanassios Fragoulis,
  • Alan J. Slusarenko and
  • Martin C. H. Gruhlke

20 May 2020

The oxidative stress response (OSR) in yeast is under the control of oxidation-sensitive cysteines in the Yap1p transcription factor, and fusion of the Yap1p-dependent OS-induced promoter of the YKL071w gene (OSI1) to a luciferase coding sequence mak...

  • Article
  • Open Access
54 Citations
8,920 Views
18 Pages

Identification of Celastrol as a Novel YAP-TEAD Inhibitor for Cancer Therapy by High Throughput Screening with Ultrasensitive YAP/TAZ–TEAD Biosensors

  • Kazem Nouri,
  • Taha Azad,
  • Min Ling,
  • Helena J. Janse van Rensburg,
  • Alexander Pipchuk,
  • He Shen,
  • Yawei Hao,
  • Jianmin Zhang and
  • Xiaolong Yang

19 October 2019

The Hippo pathway has emerged as a key signaling pathway that regulates a broad range of biological functions, and dysregulation of the Hippo pathway is a feature of a variety of cancers. Given this, some have suggested that disrupting the interactio...

  • Article
  • Open Access
2 Citations
1,861 Views
18 Pages

10 October 2024

Background: Pancreatic ductal adenocarcinoma (PDAC) is among the most aggressive forms of pancreatic cancer with a poor prognosis. YAP1 expression is markedly elevated in PDAC, but how it works is not clear. GL-V9, a derivative of the natural compoun...

  • Review
  • Open Access
1 Citations
3,052 Views
13 Pages

31 May 2023

Epithelioid haemangioendothelioma (EHE) is a rare sarcoma of the vascular endothelium with an unpredictable disease course. EHE tumours can remain indolent for long period of time but may suddenly evolve into an aggressive disease with widespread met...

  • Review
  • Open Access
1 Citations
1,735 Views
15 Pages

Gene Fusions as Potential Therapeutic Targets in Soft Tissue Sarcomas

  • Qiongdan Zheng,
  • Tong Wang,
  • Zijian Zou,
  • Wenjie Ma,
  • Zirui Dong,
  • Jingqin Zhong,
  • Wanlin Liu,
  • Yu Xu,
  • Tu Hu and
  • Wei Sun
  • + 1 author

19 June 2025

Though having been discovered in one third of sarcomas, gene fusions are less studied in their roles as potential therapeutic targets, making conventional modalities the mainstream treatment options for sarcoma patients. Recent decades have witnessed...

  • Article
  • Open Access
2 Citations
2,064 Views
13 Pages

20 September 2023

The dynamic rearrangement of the actin cytoskeleton plays an essential role in myogenesis, which is regulated by diverse mechanisms, such as mechanotransduction, modulation of the Hippo signaling pathway, control of cell proliferation, and the influe...

  • Article
  • Open Access
11 Citations
2,779 Views
25 Pages

Neuromedin S Regulates Steroidogenesis through Maintaining Mitochondrial Morphology and Function via NMUR2 in Goat Ovarian Granulosa Cells

  • Xuan Sun,
  • Cheng Zeng,
  • Feng Wang,
  • Zhen Zhang,
  • Fan Yang,
  • Zhi-Peng Liu,
  • Kang Li and
  • Guo-Min Zhang

2 November 2022

Neuromedin S (NMS) plays various roles in reproductive regulation, while the mechanism by which NMS regulates ovarian steroidogenesis remains unclear. In the current study, we confirmed the enhancement role of NMS in steroidogenesis in goat ovarian g...

  • Review
  • Open Access
3,749 Views
64 Pages

Alveolar rhabdomyosarcoma (ARMS) is a highly aggressive pediatric soft-tissue sarcoma driven by PAX3/7-FOXO1 fusion proteins. Despite intensive multimodal therapy, outcomes remain poor for patients with fusion-positive ARMS. This review integrates re...

  • Article
  • Open Access
26 Citations
5,722 Views
21 Pages

Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth

  • Daniel J. Owens,
  • Julien Messéant,
  • Sophie Moog,
  • Mark Viggars,
  • Arnaud Ferry,
  • Kamel Mamchaoui,
  • Emmanuelle Lacène,
  • Norma Roméro,
  • Astrid Brull and
  • Gisèle Bonne
  • + 2 authors

30 December 2020

Laminopathies are a clinically heterogeneous group of disorders caused by mutations in the LMNA gene, which encodes the nuclear envelope proteins lamins A and C. The most frequent diseases associated with LMNA mutations are characterized by skeletal...

  • Article
  • Open Access
1,636 Views
14 Pages

18 January 2025

An actin-binding protein, known as Calponin 3 (CNN3), modulates the remodeling of the actin cytoskeleton, a fundamental process for the maintenance of skeletal muscle homeostasis. Although the roles of CNN3 in actin remodeling have been established,...

  • Review
  • Open Access
47 Citations
10,903 Views
25 Pages

Recent Advances on Immunohistochemistry and Molecular Biology for the Diagnosis of Adnexal Sweat Gland Tumors

  • Nicolas Macagno,
  • Pierre Sohier,
  • Thibault Kervarrec,
  • Daniel Pissaloux,
  • Marie-Laure Jullie,
  • Bernard Cribier and
  • Maxime Battistella

18 January 2022

Cutaneous sweat gland tumors are a subset of adnexal neoplasms that derive or differentiate into the sweat apparatus. Their great diversity, rarity, and complex terminology make their pathological diagnosis challenging. Recent findings have revealed...

  • Article
  • Open Access
24 Citations
5,289 Views
14 Pages

Molecular Profiling of Atypical Tenosynovial Giant Cell Tumors Reveals Novel Non-CSF1 Fusions

  • Theodore Vougiouklakis,
  • Guomiao Shen,
  • Xiaojun Feng,
  • Syed T. Hoda and
  • George Jour

31 December 2019

Tenosynovial giant cell tumor (TGCT) is a benign neoplasm characterized by recurrent fusions involving the colony-stimulating factor 1 (CSF1) gene and translocation partners including collagen type VI alpha 3 chain (COL6A3) or S100 calcium-binding pr...

  • Article
  • Open Access
538 Views
10 Pages

Novel MAML2 Fusions in Human Malignancy

  • Takefumi Komiya,
  • Kieran Sweeney,
  • Chao H. Huang,
  • Anthony Crymes,
  • Emmanuel S. Antonarakis,
  • Andrew Elliott,
  • Matthew J. Oberley and
  • Mark G. Evans

27 September 2025

Background: Oncogenic fusions of MAML2 with CRTC1, CRTC3, YAP1, and NR1D1 retain the MAML2 transactivating domain (TAD) and are believed to drive aberrant gene transcription. While the oncogenic roles of these known fusions have been established, we...

  • Review
  • Open Access
5 Citations
2,747 Views
15 Pages

Porocarcinoma (PC) is a rare adnexal tumor, mainly found in the elderly. The tumor arises from the acrosyringium of eccrine sweat glands. The risk of lymph node and distant metastasis is high. Differential diagnosis with squamous cell carcinoma is di...

  • Article
  • Open Access
6 Citations
3,783 Views
20 Pages

Establishment and Characterization of a Cell Line (S-RMS1) Derived from an Infantile Spindle Cell Rhabdomyosarcoma with SRF-NCOA2 Fusion Transcript

  • Marta Colletti,
  • Angela Galardi,
  • Evelina Miele,
  • Virginia Di Paolo,
  • Ida Russo,
  • Cristiano De Stefanis,
  • Rita De Vito,
  • Martina Rinelli,
  • Andrea Ciolfi and
  • Biagio De Angelis
  • + 7 authors

Background: Spindle cell rhabdomyosarcoma (S-RMS) is a rare tumor that was previously considered as an uncommon variant of embryonal RMS (ERMS) and recently reclassified as a distinct RMS subtype with NCOA2, NCOA1, and VGLL2 fusion genes. In this stu...

  • Review
  • Open Access
5 Citations
3,511 Views
17 Pages

TFE3-Rearranged Tumors of the Kidney: An Emerging Conundrum

  • Anna Caliò,
  • Stefano Marletta,
  • Matteo Brunelli,
  • Pietro Antonini,
  • Filippo Maria Martelli,
  • Lisa Marcolini,
  • Lavinia Stefanizzi and
  • Guido Martignoni

4 October 2024

Background: Identical translocations involving the TFE3 gene and various partners have been found in both renal and soft tissue tumors, like alveolar soft part sarcoma (ASPSCR1), ossifying fibromyxoid tumor (PHF1), epithelioid hemangioendothelioma, a...

  • Article
  • Open Access
60 Citations
6,906 Views
15 Pages

Glucagon-Like Peptide-1 Receptor Agonist Attenuates Autophagy to Ameliorate Pulmonary Arterial Hypertension through Drp1/NOX- and Atg-5/Atg-7/Beclin-1/LC3β Pathways

  • Yi-Chia Wu,
  • Wei-Ting Wang,
  • Su-Shin Lee,
  • Yur-Ren Kuo,
  • Ya-Chin Wang,
  • Shih-Jung Yen,
  • Mei-Yueh Lee and
  • Jwu-Lai Yeh

Mitochondrial dysfunction is associated with cardiovascular diseases and diabetes. Pulmonary arterial hypertension (PAH) is characterized by pulmonary vascular remodeling, and the abnormal proliferation, apoptosis and migration of pulmonary arterial...

  • Review
  • Open Access
761 Views
26 Pages

The Dual Role of RASSF4 in Tumorigenesis: Mechanisms and Epigenetic Targeting Strategies

  • Rui Tian,
  • Yixin Wu,
  • Wenbin Yuan,
  • Lingli Tian,
  • Rui Zhang,
  • Hao Lyu,
  • Shuai Xiao,
  • Dong Guo,
  • Qi Zhang and
  • Declan William Ali
  • + 4 authors

18 September 2025

RASSF4 is a key member of the Ras-associated domain family (RASSF) that exhibits dual functionality in tumorigenesis, playing critical yet context-dependent roles in various malignancies. Its expression is epigenetically regulated through promoter hy...