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From Histology to Multi-Omics: Review of Chordoma Classification and Its Clinical Implications [PDF]

open access: yesCells
Chordoma is a rare malignant neoplasm of the axial skeleton, arising from notochordal remnants. No approved systemic therapies exist, and the 10-year overall survival is below 60%.
Szymon Piotr Baluszek   +2 more
doaj   +2 more sources

CHI3L1 Expression in Chordoma: Implications for Immunotherapeutic Intervention [PDF]

open access: yesCells
Chordomas are rare, highly morbid tumors arising from notochordal progenitor cells along the spinal axis, associated with severe neurological complications and high recurrence rates.
Beatrice Campilan   +17 more
doaj   +2 more sources

Chordoma [PDF]

open access: yesArchives of Pathology & Laboratory Medicine, 2021
Context.— Chordomas are uncommon malignant neoplasms with notochordal differentiation encountered by neuropathologists, bone/soft tissue pathologists, and general surgical pathologists. These lesions most commonly arise in the axial skeleton.
Veronica, Ulici, Jesse, Hart
openaire   +2 more sources

Mapping the landscape of genetic dependencies in chordoma

open access: yesNature Communications, 2023
Cancer cells possess unique molecular features that can confer an increased dependence on specific genes. Here, the authors use CRISPR-Cas9 screens to identify selectively essential genes and therapeutic targets in chordoma.
Tanaz Sharifnia   +15 more
doaj   +1 more source

Chordoma recruits and polarizes tumor-associated macrophages via secreting CCL5 to promote malignant progression

open access: yesJournal for ImmunoTherapy of Cancer, 2023
Background Chordoma is an extremely rare, locally aggressive malignant bone tumor originating from undifferentiated embryonic remnants. There are no effective therapeutic strategies for chordoma.
Wei Wang   +14 more
doaj   +1 more source

Activity of pemetrexed in pre-clinical chordoma models and humans

open access: yesScientific Reports, 2023
Chordomas are rare slow growing tumors, arising from embryonic remnants of notochord with a close predilection for the axial skeleton. Recurrence is common and no effective standard medical therapy exists.
Santosh Kesari   +14 more
doaj   +1 more source

PALB2 as a factor to predict the prognosis of patients with skull base chordoma

open access: yesFrontiers in Oncology, 2022
ObjectiveThis study aimed to study the role of PALB2 on the prognosis of skull base chordoma patients and the proliferation, migration, and invasion of chordoma cells.
Yujia Xiong   +8 more
doaj   +1 more source

Epidemiologic trend of mobile spine and sacrum chordoma: A National population-based study

open access: yesJournal of Craniovertebral Junction and Spine, 2020
Introduction: Chordoma is a rare sarcoma of the axial skeleton. The incidence of this tumor is different between races. To understand the epidemiologic characteristic and due to rarity of this pathology, large number of cases should be evaluated through ...
Mohammadreza Chehrassan   +5 more
doaj   +1 more source

DEPDC1B regulates the progression of human chordoma through UBE2T-mediated ubiquitination of BIRC5

open access: yesCell Death and Disease, 2021
Chordoma is a rare bone malignancy with a high rate of local recurrence and distant metastasis. Although DEP domain-containing protein 1B (DEPDC1B) is implicated in a variety of malignancies, its relationship with chordoma is unclear.
Liang Wang   +8 more
doaj   +1 more source

Prognostic Significance of Cyclin E1 Expression in Patients With Chordoma: A Clinicopathological and Immunohistochemical Study

open access: yesFrontiers in Oncology, 2020
PurposeChordomas are rare, slow-growing sarcomas without any accepted prognostic biomarkers. Owing to their proximity to critical neurovascular structures, discovering predictive biomarkers in chordoma has been a significant research effort because it ...
Ran Wei   +7 more
doaj   +1 more source

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