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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

Human eosinophils exert antitumorigenic effects on chordoma [PDF]

open access: yesChinese Neurosurgical Journal
Background Chordoma is a devastating rare tumor with a poor prognosis, limited therapeutic options and a high recurrence rate. The exploration of novel therapeutic targets has important clinical significance in chordoma diagnosis, treatment, and outcome ...
Wang Ying   +6 more
doaj   +2 more sources

Ubiquitin-independent pathway regulates the RIT1-MAPK pathway in chordoma progression [PDF]

open access: yesCell Death and Disease
Chordoma is a rare, slow-growing malignant tumor originating from embryonic notochord remnants and is often found in the sacrum or skull base. It is categorized into conventional, poorly differentiated, and dedifferentiated types, with the conventional ...
Hui Chen   +10 more
doaj   +2 more sources

CD3L1 expression and its association with the tumor microenvironment in 62 cases of osteosarcoma and Chordoma [PDF]

open access: yesScientific Reports
CD3L1 (ITPRIPL1), a natural ligand of CD3ε, is implicated in tumor-immune interactions and is overexpressed in several solid tumors. However, its expression and functional significance in osteosarcoma and chordoma remain uncharacterized. This study aimed
Yuhang Wang   +8 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

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

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

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

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