Advances in cancer research最新文献

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Plasticity in cell adhesion during tumor progression. 肿瘤进展过程中细胞粘附的可塑性。
Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-06-23 DOI: 10.1016/bs.acr.2025.06.001
Arka Saha, Avri Ben-Ze'ev
{"title":"Plasticity in cell adhesion during tumor progression.","authors":"Arka Saha, Avri Ben-Ze'ev","doi":"10.1016/bs.acr.2025.06.001","DOIUrl":"10.1016/bs.acr.2025.06.001","url":null,"abstract":"<p><p>Cell adhesion molecules (CAMs) mediate cellular adhesions to neighboring cells and the extracellular matrix (ECM) to regulate tissue homeostasis and morphogenesis. Dysfunctional CAM-mediated signaling is required for a neoplastic cell to gain an invasive and metastatic phenotype. Numerous studies have reported a dynamic plasticity in the function and expression of CAMs that regulates the different stages of tumor progression. As such, CAM-induced changes in cell adhesion and intracellular signaling enable phenotype switching and cellular plasticity in cancer cells that contribute to tumor aggressiveness and metastasis. This review summarizes the properties of cell adhesion molecules and the signaling pathways involved in regulating tumor progression and metastasis.</p>","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"168 ","pages":"1-61"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145535158","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Liquid biopsy in early detection and monitoring of CNS metastases. 液体活检在早期发现和监测中枢神经系统转移中的作用。
Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-05-21 DOI: 10.1016/bs.acr.2025.04.007
Natasha Hongsermeier-Graves, Mohammed Hasen, Noah Yaffe, Andrew Ajisebutu, Rachna Malani
{"title":"Liquid biopsy in early detection and monitoring of CNS metastases.","authors":"Natasha Hongsermeier-Graves, Mohammed Hasen, Noah Yaffe, Andrew Ajisebutu, Rachna Malani","doi":"10.1016/bs.acr.2025.04.007","DOIUrl":"10.1016/bs.acr.2025.04.007","url":null,"abstract":"<p><p>The treatment of human cancer has shifted toward a precision-medicine paradigm that increasingly relies on the genomic annotation of each patient's tumor tissue. This trend is supported by the observation that treatment response is often dependent on tumor mutations in targeted pathways, by the discovery of particular drug-resistance mutations in tumors that resume growth during therapy, and by the recent association between effective immunotherapy and tumor-specific missense mutations. Early detection of cancer and accurate characterization of tumors improve patient outcomes, so research into noninvasive means of obtaining this information is of significant clinical relevance. Furthermore, the outgrowth of drug-resistant tumor cell clones during therapy can limit the clinical relevance of the initial tumor profile and has motivated the development of technologies that can track the evolution of the cancer genome in accessible body fluids.</p>","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"165 ","pages":"255-290"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144304207","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Craniopharyngioma. 颅咽管瘤。
Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-10-20 DOI: 10.1016/bs.acr.2025.09.005
Eric Montgomery, Siddhartha Mitra, Cassie Kline, Todd C Hankinson
{"title":"Craniopharyngioma.","authors":"Eric Montgomery, Siddhartha Mitra, Cassie Kline, Todd C Hankinson","doi":"10.1016/bs.acr.2025.09.005","DOIUrl":"10.1016/bs.acr.2025.09.005","url":null,"abstract":"<p><p>Introduction Adamantinomatous craniopharyngioma (ACP) is a significant source of morbidity in the pediatric brain tumor population. It predominantly arises from the parasellar space. The tumors proximity to key vital structures often makes gross total surgical resection challenging and sometimes clinically inadvisable. Compounding the problem, adjunct therapies are not yet capable of providing a definitive cure. Recent preclinical research has made significant progress towards elucidating the mutagenic drivers of ACP, however much work remains to translate this into safe and effective treatments. Content Overview and Key Takeaways In the following chapter, we discuss the most up-to-date understanding of ACP biology and management. ACP is a histologically low grade tumor characterized by a mutation involving the beta-catenin protein, resulting in pathologic stability of the protein that impairs cell death or apoptosis. A subpopulation of tumor cells then enter a transcriptomic state characterized by cellular oncogenic senescence. It is unclear how this state leads to feed forward loops resulting in tumorigenesis. Despite its benign nature, the consistent anatomic origin of ACP in the sellar/suprasellar space, often abutting or involving the hypothalamus, the infundibulum, and the optic chiasm, contributes to multiple long-term complications such as endocrinopathies, obesity, vision loss, and obstructive hydrocephalus. Surgically, the current trend is towards conservative approaches with the goal of maximal safe resection without perturbing the hypothalamus. Adjunct radiotherapy is standard in cases of residual or recurrent disease. Close coordination with endocrinology colleagues is vital to appropriately care for these patients as they often suffer from lifelong endocrinopathies that remain a significant source of burden in this population.</p>","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"167 ","pages":"243-277"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145461266","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An overview of the diagnosis and management of Choroid Plexus tumors. 脉络膜丛肿瘤的诊断和治疗综述。
Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-09-20 DOI: 10.1016/bs.acr.2025.08.008
Diana S Osorio, Maxim Yankelevich, Lucie Lafay-Cousin, Wafik Zaky
{"title":"An overview of the diagnosis and management of Choroid Plexus tumors.","authors":"Diana S Osorio, Maxim Yankelevich, Lucie Lafay-Cousin, Wafik Zaky","doi":"10.1016/bs.acr.2025.08.008","DOIUrl":"10.1016/bs.acr.2025.08.008","url":null,"abstract":"<p><p>Choroid Plexus Tumors (CPT) are rare (2-4% of all pediatric CNS tumors), predominantly early childhood brain neoplasms. Due to their rarity and the lack of prospective clinical trials, evidence-based treatment guidelines remain limited. This review provides a comprehensive summary of the current knowledge.nnCPTs span a spectrum from mature Choroid Plexus Papillomas (CPP) to malignant Choroid Plexus Carcinomas (CPC), with Atypical Choroid Plexus Papillomas (aCPP) in between. A significant proportion of CPCs are driven by either somatic or germline TP53 mutations (Li-Fraumeni syndrome); however, other molecular drivers of CPT tumorigenesis remain poorly understood. CPTs exhibit distinct DNA methylation profiles, allowing for classification into clinically relevant subgroups. These tumors also display a chromosomal instability phenotype, characterized by multiple copy number alterations. nnAdvances in molecular profiling have revealed that TP53-mutated CPCs have significantly worse outcomes. Both retrospective and limited prospective data have shown 5-year event-free survival rates of 0-25% for TP53-mutant CPCs versus 70-80% for TP53-wild-type cases. The extent of surgical resection remains another established prognostic factor, while data on the roles of radiation therapy (RT) and myeloablative chemotherapy with stem cell rescue are still evolving. Preliminary evidence suggests that TP53-mutant patients may be getting less benefit from RT, but greater benefit from myeloablative chemotherapy approach with avoidance of RT.nn The emerging insights into CPC biology and long-term outcomes can direct the design of future clinical trials. A new international prospective study led by the Pediatric Neuro-Oncology Consortium is in development, with the goal to stratify patients by molecular subtype to receive different therapy based on individual molecular profiles and patient age.</p>","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"167 ","pages":"103-139"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145461267","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Michael addition drugs and cancer. 迈克尔增加了毒品和癌症。
Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-06-24 DOI: 10.1016/bs.acr.2025.06.004
Kenneth D Tew, Danyelle M Townsend, Leilei Zhang, Xuhong Zhang, Zhiwei Ye, Jie Zhang
{"title":"Michael addition drugs and cancer.","authors":"Kenneth D Tew, Danyelle M Townsend, Leilei Zhang, Xuhong Zhang, Zhiwei Ye, Jie Zhang","doi":"10.1016/bs.acr.2025.06.004","DOIUrl":"10.1016/bs.acr.2025.06.004","url":null,"abstract":"<p><p>Some of the earliest anticancer drugs were alkylating agents, capable of covalently modifying critical cellular nucleophiles in proteins and nucleic acids. For many years, adapting another type of covalent reaction, Michael addition reactions, which involve the nucleophilic attack of a carbon nucleophile on an α,β-unsaturated carbonyl compound, have been explored in designing covalent inhibitors that selectively target cancer-related biomolecules. Numerous natural products demonstrate Michael addition properties, contributing to their bioactivity in antioxidant, anti-inflammatory and anticancer mechanisms. These compounds often interact with cellular nucleophiles, modulating redox signaling, enzyme catalysis, and stress response pathways. In the context of cancer treatments, several FDA-approved drugs, including proteostatic, EGFR and Ras inhibitors, employ Michael addition chemistry to achieve irreversible inhibition of cancer-related targets. The review emphasizes the challenges associated with these drugs, including off-target effects, toxicity, and drug resistance, but highlights some advances in medicinal chemistry that have improved selectivity and therapeutic efficacy. There are emerging covalent inhibitors that leverage Michael addition to enhance cancer treatment, underscoring the ongoing efforts to refine these compounds for clinical translation. Overall, this review examines the mechanisms, applications, and therapeutic potentials of Michael addition drugs in oncology, alongside relevant literature, and clinical findings.</p>","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"168 ","pages":"196-220"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145535175","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preface. 前言。
Advances in cancer research Pub Date : 2025-01-01 DOI: 10.1016/S0065-230X(25)00042-9
Mariza Daras, David D Limbrick, Paul B Fisher
{"title":"Preface.","authors":"Mariza Daras, David D Limbrick, Paul B Fisher","doi":"10.1016/S0065-230X(25)00042-9","DOIUrl":"https://doi.org/10.1016/S0065-230X(25)00042-9","url":null,"abstract":"","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"166 ","pages":"xiii-xvi"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144661504","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preface. 前言。
Advances in cancer research Pub Date : 2025-01-01 DOI: 10.1016/S0065-230X(25)00070-3
Mohamed S Abdelbaki, Paul B Fisher, David D Limbrick
{"title":"Preface.","authors":"Mohamed S Abdelbaki, Paul B Fisher, David D Limbrick","doi":"10.1016/S0065-230X(25)00070-3","DOIUrl":"https://doi.org/10.1016/S0065-230X(25)00070-3","url":null,"abstract":"","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"167 ","pages":"xvii-xxii"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145460665","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Molecular drivers in primary brain tumor formation. 原发性脑肿瘤形成的分子驱动因素。
Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-04-25 DOI: 10.1016/bs.acr.2025.04.006
Hope T Richard
{"title":"Molecular drivers in primary brain tumor formation.","authors":"Hope T Richard","doi":"10.1016/bs.acr.2025.04.006","DOIUrl":"10.1016/bs.acr.2025.04.006","url":null,"abstract":"<p><p>Gliomas are a common form of intracranial malignancy in adults with poor overall survival and limited treatment strategies. There is significant genetic heterogeneity in this tumor group with a complex network of signaling that leads to rapid infiltrative growth as well as chemo- and radio-resistance. This chapter will delve into the complex processes and molecular alterations that feed into the formation and growth of these primary brain tumors.</p>","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"166 ","pages":"1-32"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144661438","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Molecular drivers in CNS metastatic disease. 中枢神经系统转移性疾病的分子驱动因素。
Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-04-30 DOI: 10.1016/bs.acr.2025.04.004
Hannah Kim, Sofia Chernet, Priya Kumthekar, Akanksha Sharma
{"title":"Molecular drivers in CNS metastatic disease.","authors":"Hannah Kim, Sofia Chernet, Priya Kumthekar, Akanksha Sharma","doi":"10.1016/bs.acr.2025.04.004","DOIUrl":"10.1016/bs.acr.2025.04.004","url":null,"abstract":"<p><p>The incidence and prevalence of CNS metastases of systemic cancer is only increasing worldwide, especially as our available systemic therapies have improved, resulting in longer survival and more time to allow for CNS progression. Fortunately, we have made substantial therapeutic advances in drug development in the last decade, with newer agents demonstrating significant penetration into the nervous system and notable efficacy. Treatments specifically targeted for certain mutations in the cancer pathway have been especially successful in aborting the onward trajectory and growth of cancer cells in the nervous system. In this review, we provide an overview and update of the drugs that have demonstrated benefit in achieving intracranial control (at times including leptomeningeal disease), many of which have already received or are pending regulatory approval. We also provide a brief look into the landscape of ongoing clinical research including challenges in the field.</p>","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"165 ","pages":"1-56"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144304246","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In search of a targetable immune profile for acute myeloid leukemia. 寻找急性髓性白血病的可靶向免疫谱。
Advances in cancer research Pub Date : 2025-01-01 Epub Date: 2025-07-12 DOI: 10.1016/bs.acr.2025.06.005
Gurnit Kaur, Negar Ghaffari, Nagesh Kalakonda, William Grey, Vanessa Marensi
{"title":"In search of a targetable immune profile for acute myeloid leukemia.","authors":"Gurnit Kaur, Negar Ghaffari, Nagesh Kalakonda, William Grey, Vanessa Marensi","doi":"10.1016/bs.acr.2025.06.005","DOIUrl":"10.1016/bs.acr.2025.06.005","url":null,"abstract":"<p><p>Acute myeloid leukemia is a poor prognostic blood cancer with dismal survival rates. Major challenges in improving AML survivorship include its heterogeneity and ability to evade immunosurveillance. To facilitate subtyping and therapeutic decision-making, AML is risk stratified according to the genetic landscape, however, less is known about phenotypic differences and immune receptor signatures. Immune profiling of cancer cells is complex and a key determinant of tumor progression. In addition to influencing disease management, an understanding of cell surface immune receptor profiles provides key information on how different AML subgroups evade surveillance. Several robust studies aimed at characterizing the immune profile of cancer cells and gaining a deeper understanding of their function as cellular markers, have provided key information within the field. This review aims to compile information on the immune profiles of AML, understand their role in immune evasion, therapy responses, recurrence, and outcomes.</p>","PeriodicalId":94294,"journal":{"name":"Advances in cancer research","volume":"168 ","pages":"159-194"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145535166","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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