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  1. Article ; Online: Understanding and targeting prostate cancer cell heterogeneity and plasticity.

    Tang, Dean G

    Seminars in cancer biology

    2021  Volume 82, Page(s) 68–93

    Abstract: ... This inherent PCa cell heterogeneity, e.g., in the expression of androgen receptor (AR), constitutes a barrier ...

    Abstract Prostate cancer (PCa) is a prevalent malignancy that occurs primarily in old males. Prostate tumors in different patients manifest significant inter-patient heterogeneity with respect to histo-morphological presentations and molecular architecture. An individual patient tumor also harbors genetically distinct clones in which PCa cells display intra-tumor heterogeneity in molecular features and phenotypic marker expression. This inherent PCa cell heterogeneity, e.g., in the expression of androgen receptor (AR), constitutes a barrier to the long-term therapeutic efficacy of AR-targeting therapies. Furthermore, tumor progression as well as therapeutic treatments induce PCa cell plasticity such that AR-positive PCa cells may turn into AR-negative cells and prostate tumors may switch lineage identity from adenocarcinomas to neuroendocrine-like tumors. This induced PCa cell plasticity similarly confers resistance to AR-targeting and other therapies. In this review, I first discuss PCa from the perspective of an abnormal organ development and deregulated cellular differentiation, and discuss the luminal progenitor cells as the likely cells of origin for PCa. I then focus on intrinsic PCa cell heterogeneity in treatment-naïve tumors with the presence of prostate cancer stem cells (PCSCs). I further elaborate on PCa cell plasticity induced by genetic alterations and therapeutic interventions, and present potential strategies to therapeutically tackle PCa cell heterogeneity and plasticity. My discussions will make it clear that, to achieve enduring clinical efficacy, both intrinsic PCa cell heterogeneity and induced PCa cell plasticity need to be targeted with novel combinatorial approaches.
    MeSH term(s) Adenocarcinoma/genetics ; Cell Line, Tumor ; Cell Plasticity ; Humans ; Male ; Neoplastic Stem Cells/metabolism ; Prostatic Neoplasms/drug therapy ; Prostatic Neoplasms/genetics ; Prostatic Neoplasms/metabolism ; Receptors, Androgen/genetics ; Receptors, Androgen/metabolism
    Chemical Substances Receptors, Androgen
    Language English
    Publishing date 2021-11-26
    Publishing country England
    Document type Journal Article ; Review ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 1033980-2
    ISSN 1096-3650 ; 1044-579X
    ISSN (online) 1096-3650
    ISSN 1044-579X
    DOI 10.1016/j.semcancer.2021.11.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Cancer cell heterogeneity and plasticity: From molecular understanding to therapeutic targeting.

    Tang, Dean G / Kondo, Toru

    Seminars in cancer biology

    2021  Volume 82, Page(s) 1–2

    MeSH term(s) Cell Plasticity ; Humans ; Neoplasms/drug therapy ; Neoplasms/genetics ; Neoplastic Stem Cells
    Language English
    Publishing date 2021-10-06
    Publishing country England
    Document type Editorial ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 1033980-2
    ISSN 1096-3650 ; 1044-579X
    ISSN (online) 1096-3650
    ISSN 1044-579X
    DOI 10.1016/j.semcancer.2021.10.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: "Splice" a way towards neuroendocrine prostate cancer.

    Zhang, Dingxiao / Tang, Dean G

    EBioMedicine

    2018  Volume 35, Page(s) 12–13

    MeSH term(s) Carcinoma, Neuroendocrine ; Humans ; Male ; Prostatic Neoplasms
    Language English
    Publishing date 2018-08-31
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S. ; Comment
    ZDB-ID 2851331-9
    ISSN 2352-3964
    ISSN (online) 2352-3964
    DOI 10.1016/j.ebiom.2018.08.037
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: ULM-MbCNRT: In vivo Ultrafast Ultrasound Localization Microscopy by Combining Multi-branch CNN and Recursive Transformer.

    Zhang, Gaobo / Gu, Wenting / Yue, Yaoting / Tang, Meng-Xing / Luo, Jianwen / Liu, Xin / Ta, Dean

    IEEE transactions on ultrasonics, ferroelectrics, and frequency control

    2024  Volume PP

    Abstract: ... compared to the previous DL method (e.g., the modified sub-pixel convolutional neural network, ULM-mSPCN ...

    Abstract Ultrasound localization microscopy (ULM) overcomes the acoustic diffraction limit by localizing tiny microbubbles (MBs), thus enabling the microvascular to be rendered at sub-wavelength resolution. Nevertheless, to obtain such superior spatial resolution, it is necessary to spend tens of seconds gathering numerous ultrasound (US) frames to accumulate MB events required, resulting in ULM imaging still suffering from trade-offs between imaging quality, data acquisition time and data processing speed. In this paper, we present a new deep learning (DL) framework combining multi-branch CNN and recursive Transformer, termed as ULM-MbCNRT, that is capable of reconstructing a super-resolution image directly from a temporal mean low-resolution image generated by averaging much fewer raw US frames, i.e., implement an ultrafast ULM imaging. To evaluate the performance of ULM-MbCNRT, a series of numerical simulations and in vivo experiments are carried out. Numerical simulation results indicate that ULM-MbCNRT achieves high-quality ULM imaging with ~10-fold reduction in data acquisition time and ~130-fold reduction in computation time compared to the previous DL method (e.g., the modified sub-pixel convolutional neural network, ULM-mSPCN). For the in vivo experiments, when comparing to the ULM-mSPCN, ULM-MbCNRT allows ~37-fold reduction in data acquisition time (~0.8 s) and ~2134-fold reduction in computation time (~0.87 s) without sacrificing spatial resolution. It implies that ultrafast ULM imaging holds promise for observing rapid biological activity in vivo, potentially improving the diagnosis and monitoring of clinical conditions.
    Language English
    Publishing date 2024-04-12
    Publishing country United States
    Document type Journal Article
    ISSN 1525-8955
    ISSN (online) 1525-8955
    DOI 10.1109/TUFFC.2024.3388102
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Androgen receptor (AR) heterogeneity in prostate cancer and therapy resistance.

    Jamroze, Anmbreen / Chatta, Gurkamal / Tang, Dean G

    Cancer letters

    2021  Volume 518, Page(s) 1–9

    Abstract: Androgen receptor (AR), a ligand-dependent nuclear transcription factor and a member of steroid hormone receptor family, plays an important role in prostate organogenesis by regulating epithelial differentiation and restricting cell proliferation. ... ...

    Abstract Androgen receptor (AR), a ligand-dependent nuclear transcription factor and a member of steroid hormone receptor family, plays an important role in prostate organogenesis by regulating epithelial differentiation and restricting cell proliferation. Although rarely mutated or amplified in treatment-naïve prostate cancer (PCa), AR signaling drives tumor growth and as a result, therapies that aim to inhibit AR signaling, called ARSIs (AR signaling inhibitors), have been in clinical use for >70 years. Unfortunately, the clinical efficacy of ARSIs is short-lived and the majority of treated patients develop castration-resistant PCa (CRPC). Numerous molecular mechanisms have been proposed for castration resistance; however, the cellular basis for CRPC emergence has remained obscure. One under-appreciated cellular mechanism for CRPC development is the AR heterogeneity that pre-exists in treatment-naive primary tumors, i.e., although most PCa cells express AR (i.e., AR
    MeSH term(s) Cell Proliferation/physiology ; Drug Resistance, Neoplasm/physiology ; Humans ; Male ; Prostate/metabolism ; Prostatic Neoplasms/metabolism ; Receptors, Androgen/metabolism ; Signal Transduction/physiology
    Chemical Substances Receptors, Androgen
    Language English
    Publishing date 2021-06-10
    Publishing country Ireland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S. ; Review
    ZDB-ID 195674-7
    ISSN 1872-7980 ; 0304-3835
    ISSN (online) 1872-7980
    ISSN 0304-3835
    DOI 10.1016/j.canlet.2021.06.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: MicroRNA-34a, Prostate Cancer Stem Cells, and Therapeutic Development.

    Li, Wen Jess / Liu, Xiaozhuo / Dougherty, Emily M / Tang, Dean G

    Cancers

    2022  Volume 14, Issue 18

    Abstract: Prostate cancer (PCa) is a highly heterogeneous disease and typically presents with multiple distinct cancer foci. Heterogeneity in androgen receptor (AR) expression levels in PCa has been observed for decades, from untreated tumors to castration- ... ...

    Abstract Prostate cancer (PCa) is a highly heterogeneous disease and typically presents with multiple distinct cancer foci. Heterogeneity in androgen receptor (AR) expression levels in PCa has been observed for decades, from untreated tumors to castration-resistant prostate cancer (CRPC) to disseminated metastases. Current standard-of-care therapies for metastatic CRPC can only extend life by a few months. Cancer stem cells (CSCs) are defined as a subpopulation of cancer cells that exists in almost all treatment-naive tumors. Additionally, non-CSCs may undergo cellular plasticity to be reprogrammed to prostate cancer stem cells (PCSCs) during spontaneous tumor progression or upon therapeutic treatments. Consequently, PCSCs may become the predominant population in treatment-resistant tumors, and the "root cause" for drug resistance. microRNA-34a (miR-34a) is a bona fide tumor-suppressive miRNA, and its expression is dysregulated in PCa. Importantly, miR-34a functions as a potent CSC suppressor by targeting many molecules essential for CSC survival and functions, which makes it a promising anti-PCSC therapeutic. Here, we conducted a comprehensive literature survey of miR-34a in the context of PCa and especially PCSCs. We provided an updated overview on the mechanisms of miR-34a regulation followed by discussing its tumor suppressive functions in PCa. Finally, based on current advances in miR-34a preclinical studies in PCa, we offered potential delivery strategies for miR-34a-based therapeutics for treating advanced PCa.
    Language English
    Publishing date 2022-09-19
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14184538
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Cancers of the breast and prostate: a stem cell perspective.

    Tang, Dean G

    Endocrine-related cancer

    2015  Volume 22, Issue 6, Page(s) E9–E11

    MeSH term(s) Animals ; Breast Neoplasms/pathology ; Cell Transformation, Neoplastic ; Epithelial Cells/pathology ; Female ; Gonadal Steroid Hormones ; Humans ; Hyperplasia ; Male ; Mammary Neoplasms, Experimental/pathology ; Mice ; Neoplasms, Hormone-Dependent/pathology ; Neoplastic Stem Cells/pathology ; Organ Specificity ; Prostatic Neoplasms/pathology
    Chemical Substances Gonadal Steroid Hormones
    Language English
    Publishing date 2015-12
    Publishing country England
    Document type Editorial ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1218450-0
    ISSN 1479-6821 ; 1351-0088
    ISSN (online) 1479-6821
    ISSN 1351-0088
    DOI 10.1530/ERC-15-0427
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Systematic review and meta-analysis of topical tranexamic acid in spine surgery.

    Izima, Chiemela / Sampath, Shailen G / Tang, Anthony J / Ambati, Vardhaan S / Chou, Dean / Chan, Andrew K

    Neurosurgical focus

    2023  Volume 55, Issue 4, Page(s) E18

    Abstract: Objective: Tranexamic acid (TXA) is an antifibrinolytic drug associated with reduced blood loss in a range of surgical specialties, including neurosurgery, orthopedic surgery, and cardiac surgery. Concerns about venous thromboembolism and seizures from ... ...

    Abstract Objective: Tranexamic acid (TXA) is an antifibrinolytic drug associated with reduced blood loss in a range of surgical specialties, including neurosurgery, orthopedic surgery, and cardiac surgery. Concerns about venous thromboembolism and seizures from intravenous (IV) TXA have led to increased use of topical TXA. Given the relative scarcity of the literature on topical TXA compared with that on IV TXA within neurosurgery, the authors aimed to conduct a systematic review and meta-analysis on the safety, efficacy, and optimal administration of topical TXA in a wide range of spinal procedures and pathologies.
    Methods: The PRISMA guidelines, Cochrane risk of bias tool, and Newcastle-Ottawa Scale were used to extract randomized controlled trials and high-quality case-control and cross-sectional/cohort studies (adult studies only) from PubMed, Web of Science, Cochrane Library, and Embase published between 2016 and 2023. Studies were analyzed by two independent reviewers for variables including dosage, TXA administration route, type of spine procedure, blood loss, adverse events including thromboembolism and infection, postoperative hemoglobin level, and hospitalization length. Pooled analysis comparing intraoperative and postoperative blood loss, postoperative hemoglobin levels, and hospitalization length of stay on the basis of route of TXA administration was conducted.
    Results: Four cohort studies, 1 cross-sectional study, 1 case-control study, and 12 randomized controlled trials, together involving 2045 patients, were included. The most common route of topical TXA administration was via TXA in saline solution. Other routes of topical TXA included retrograde injection and TXA-soaked Gelfoam. In pooled analysis, topical TXA significantly reduced visible blood loss (standardized mean difference [SMD] -0.22, 95% CI -0.45 to -0.00001), postoperative blood loss (SMD -1.63, 95% CI -2.03 to -1.22), and length of hospital stay (SMD -1.02, 95% CI -1.42 to -0.61), as well as higher postoperative hemoglobin (SMD 0.59, 95% CI 0.34-0.83), compared with non-TXA controls. No significant differences in outcomes were found between topical and IV TXA or between combined (topical and IV) and IV TXA. Thromboembolism and infection rates did not significantly differ between any TXA administration group and non-TXA controls.
    Conclusions: In pooled analyses, topical TXA was associated with decreased perioperative blood loss in a wide range of scenarios, including cervical spine surgery and thoracolumbar trauma, as well as in patients with a thromboembolic history.
    MeSH term(s) Humans ; Tranexamic Acid/therapeutic use ; Cross-Sectional Studies ; Case-Control Studies ; Blood Loss, Surgical/prevention & control ; Postoperative Hemorrhage ; Thromboembolism/drug therapy ; Hemoglobins
    Chemical Substances Tranexamic Acid (6T84R30KC1) ; Hemoglobins
    Language English
    Publishing date 2023-10-01
    Publishing country United States
    Document type Meta-Analysis ; Systematic Review ; Journal Article
    ZDB-ID 2026589-X
    ISSN 1092-0684 ; 1092-0684
    ISSN (online) 1092-0684
    ISSN 1092-0684
    DOI 10.3171/2023.7.FOCUS23363
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Developing Folate-Conjugated miR-34a Therapeutic for Prostate Cancer: Challenges and Promises.

    Li, Wen Jess / Wang, Yunfei / Liu, Xiaozhuo / Wu, Shan / Wang, Moyi / Turowski, Steven G / Spernyak, Joseph A / Tracz, Amanda / Abdelaal, Ahmed M / Sudarshan, Kasireddy / Puzanov, Igor / Chatta, Gurkamal / Kasinski, Andrea L / Tang, Dean G

    International journal of molecular sciences

    2024  Volume 25, Issue 4

    Abstract: Prostate cancer (PCa) remains a common cancer with high mortality in men due to its heterogeneity and the emergence of drug resistance. A critical factor contributing to its lethality is the presence of prostate cancer stem cells (PCSCs), which can self- ... ...

    Abstract Prostate cancer (PCa) remains a common cancer with high mortality in men due to its heterogeneity and the emergence of drug resistance. A critical factor contributing to its lethality is the presence of prostate cancer stem cells (PCSCs), which can self-renew, long-term propagate tumors, and mediate treatment resistance. MicroRNA-34a (miR-34a) has shown promise as an anti-PCSC therapeutic by targeting critical molecules involved in cancer stem cell (CSC) survival and functions. Despite extensive efforts, the development of miR-34a therapeutics still faces challenges, including non-specific delivery and delivery-associated toxicity. One emerging delivery approach is ligand-mediated conjugation, aiming to achieve specific delivery of miR-34a to cancer cells, thereby enhancing efficacy while minimizing toxicity. Folate-conjugated miR-34a (folate-miR-34a) has demonstrated promising anti-tumor efficacy in breast and lung cancers by targeting folate receptor α (FOLR1). Here, we first show that miR-34a, a TP53 transcriptional target, is reduced in PCa that harbors
    MeSH term(s) Humans ; Male ; Cell Line, Tumor ; Cell Proliferation/genetics ; Folate Receptor 1/genetics ; Folate Receptor 1/metabolism ; Folate Receptor 1/therapeutic use ; Gene Expression Regulation, Neoplastic ; Ligands ; Lung Neoplasms/drug therapy ; Lung Neoplasms/genetics ; MicroRNAs/metabolism ; MicroRNAs/therapeutic use ; Prostatic Neoplasms/drug therapy ; Prostatic Neoplasms/genetics ; Folic Acid/pharmacology ; Folic Acid/therapeutic use
    Chemical Substances Folate Receptor 1 ; FOLR1 protein, human ; Ligands ; MicroRNAs ; MIRN34 microRNA, human ; Folic Acid (935E97BOY8)
    Language English
    Publishing date 2024-02-09
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms25042123
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Developing folate-conjugated miR-34a therapeutic for prostate cancer treatment: Challenges and promises.

    Li, Wen Jess / Wang, Yunfei / Liu, Xiaozhuo / Wu, Shan / Wang, Moyi / Turowski, Steven G / Spernyak, Joseph A / Tracz, Amanda / Abdelaal, Ahmed M / Sudarshan, Kasireddy / Puzanov, Igor / Chatta, Gurkamal / Kasinski, Andrea L / Tang, Dean G

    bioRxiv : the preprint server for biology

    2024  

    Abstract: Prostate cancer (PCa) remains a common cancer with high mortality in men due to its heterogeneity and the emergence of drug resistance. A critical factor contributing to its lethality is the presence of prostate cancer stem cells (PCSCs), which can self- ... ...

    Abstract Prostate cancer (PCa) remains a common cancer with high mortality in men due to its heterogeneity and the emergence of drug resistance. A critical factor contributing to its lethality is the presence of prostate cancer stem cells (PCSCs), which can self-renew, long-term propagate tumors and mediate treatment resistance. MicroRNA-34a (miR-34a) has shown promise as an anti-PCSC therapeutic by targeting critical molecules involved in cancer stem cell (CSC) survival and functions. Despite extensive efforts, the development of miR-34a therapeutics still faces challenges, including non-specific delivery and delivery-associated toxicity. One emerging delivery approach is ligand-mediated conjugation, aiming to achieve specific delivery of miR-34a to cancer cells, thereby enhancing efficacy while minimizing toxicity. Folate-conjugated miR-34a (folate-miR-34a) has demonstrated promising anti-tumor efficacy in breast and lung cancers by targeting folate receptor α (FOLR1). Here, we first show that miR-34a, a TP53 transcriptional target, is reduced in PCa that harbors TP53 loss or mutations and that miR-34a mimic, when transfected into PCa cells, downregulated multiple miR-34a targets and inhibited cell growth. When exploring the therapeutic potential of folate-miR-34a, we found that folate-miR-34a exhibited impressive inhibitory effects on breast, ovarian and cervical cancer cells but showed minimal effects on and targeted delivery to PCa cells due to a lack of appreciable expression of FOLR1 in PCa cells. Folate-miR-34a also did not display any apparent effect on PCa cells expressing prostate-specific membrane antigen (PMSA) despite the reported folate's binding capability to PSMA. These results highlight challenges in specific delivery of folate-miR-34a to PCa due to lack of target (receptor) expression. Our study offers novel insights on the challenges and promises within the field and cast light on the development of ligand-conjugated miR-34a therapeutics for PCa.
    Language English
    Publishing date 2024-01-21
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.11.25.568612
    Database MEDical Literature Analysis and Retrieval System OnLINE

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