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Hua Wu

Researcher at Fujian Medical University

Publications -  17
Citations -  627

Hua Wu is an academic researcher from Fujian Medical University. The author has contributed to research in topics: Medicine & Cancer. The author has an hindex of 6, co-authored 8 publications receiving 206 citations. Previous affiliations of Hua Wu include Xiamen University.

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Comparison of [68Ga]Ga-DOTA-FAPI-04 and [18F] FDG PET/CT for the diagnosis of primary and metastatic lesions in patients with various types of cancer.

TL;DR: [68Ga]Ga-DOTA-FAPI-04 PET/CT showed a superior diagnostic efficacy than [18F] FDGPET/CT for the diagnosis of primary and metastatic lesions in patients with various types of cancer, especially in identifying liver metastases, peritoneal carcinomatosis, and brain tumours.
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Usefulness of [68Ga]Ga-DOTA-FAPI-04 PET/CT in patients presenting with inconclusive [18F]FDG PET/CT findings

TL;DR: In patients undergoing oncological evaluation with inconclusive [ 18 F]FDG PET/CT findings, [ 68 Ga]Ga-DOTA-FAPI-04 may have a complementary role in discriminating mass lesions on conventional imaging, locating the primary site of unknown malignancy, modifying tumour staging, and detecting suspected disease recurrence.
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Fibroblast activation protein-based theranostics in cancer research: A state-of-the-art review

TL;DR: The literature for the state-of-the-art FAPI-PET imaging for cancer diagnosis compared with fluorodeoxyglucose (FDG)-PET is summarized and the use of FAP-PET for therapeutic regimen improvement and fibroblast activation protein (FAP)-targeted molecule modification strategies is summarized.
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[18F]FDG and [68Ga]Ga-DOTA-FAPI-04 PET/CT in the evaluation of tuberculous lesions.

TL;DR: [Ga]Ga-DOTA-FAPI-04 PET/CT showed higher tracer uptake in tuberculous lesions in the lung, spines, and brain than did [F]FDG PET/ CT; such imaging modality may be useful for determinWeipeng Huang and Haojun Chen contributed equally to this work.
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Mycoepoxydiene inhibits activation of BV2 microglia stimulated by lipopolysaccharide through suppressing NF-κB, ERK 1/2 and toll-like receptor pathways.

TL;DR: The results demonstrate that the inhibitory and promotion effect of MED on LPS-stimulated inflammatory mediators and anti-inflammatory factor production in BV2 microglia is associated with the suppression of the NF-κB, ERK1/2 and TLR signaling pathways.