CANCER BIOLOGY & THERAPY

CANCER BIOLOGY & THERAPY

癌症生物学与治疗
CANCER BIOL THER
影响因子:4.6
JCR分区:Q1
新锐分区:医学2区
是否综述期刊:N/A
是否预警:不在预警名单内
是否OA:
出版国家/地区:UNITED STATES
出版社:Landes Bioscience
发刊时间:2002
收录数据库:SCIE/Scopus收录/DOAJ开放期刊
ISSN:1538-4047

期刊介绍

Cancer, the second leading cause of death, is a heterogenous group of over 100 diseases. Cancer is characterized by disordered and deregulated cellular and stromal proliferation accompanied by reduced cell death with the ability to survive under stresses of nutrient and growth factor deprivation, hypoxia, and loss of cell-to-cell contacts. At the molecular level, cancer is a genetic disease that develops due to the accumulation of mutations over time in somatic cells. The phenotype includes genomic instability and chromosomal aneuploidy that allows for acceleration of genetic change. Malignant transformation and tumor progression of any cell requires immortalization, loss of checkpoint control, deregulation of growth, and survival. A tremendous amount has been learned about the numerous cellular and molecular genetic changes and the host-tumor interactions that accompany tumor development and progression. It is the goal of the field of Molecular Oncology to use this knowledge to understand cancer pathogenesis and drug action, as well as to develop more effective diagnostic and therapeutic strategies for cancer. This includes preventative strategies as well as approaches to treat metastases. With the availability of the human genome sequence and genomic and proteomic approaches, a wealth of tools and resources are generating even more information. The challenge will be to make biological sense out of the information, to develop appropriate models and hypotheses and to translate information for the clinicians and the benefit of their patients. Cancer Biology & Therapy aims to publish original research on the molecular basis of cancer, including articles with translational relevance to diagnosis or therapy. We will include timely reviews covering the broad scope of the journal. The journal will also publish op-ed pieces and meeting reports of interest. The goal is to foster communication and rapid exchange of information through timely publication of important results using traditional as well as electronic formats. The journal and the outstanding Editorial Board will strive to maintain the highest standards for excellence in all activities to generate a valuable resource.
癌症是死亡的第二大原因,是由100多种疾病组成的异质组。癌症的特征在于细胞和基质增殖紊乱和失调,伴随着细胞死亡减少,具有在营养和生长因子剥夺、缺氧和细胞间接触丧失的应激下存活的能力。在分子水平上,癌症是一种遗传疾病,是由于体细胞中突变随着时间的推移而积累而发展起来的。表型包括基因组不稳定性和染色体非整倍性,这使得遗传变化加速。任何细胞的恶性转化和肿瘤进展都需要永生化、检查点控制的丧失、生长失调和存活。关于伴随肿瘤发生和发展的许多细胞和分子遗传变化以及宿主-肿瘤相互作用,已经了解了大量信息。分子肿瘤学领域的目标是利用这些知识来理解癌症发病机制和药物作用,以及开发更有效的癌症诊断和治疗策略。这包括预防策略以及治疗转移的方法。随着人类基因组序列以及基因组和蛋白质组学方法的可用性,大量的工具和资源正在产生更多的信息。挑战将是从信息中获得生物学意义,开发适当的模型和假设,并为临床医生和患者的利益翻译信息。《癌症生物学与治疗》旨在发表关于癌症分子基础的原创研究,包括与诊断或治疗相关的翻译文章。我们将包括及时审查涵盖广泛的范围内的杂志。该杂志还将发表感兴趣的专栏文章和会议报告。目标是通过使用传统和电子格式及时公布重要结果,促进沟通和信息的快速交流。该杂志和杰出的编辑委员会将努力保持最高标准的卓越的所有活动,以产生宝贵的资源。
年发文量 110
国人发稿量 60.5
国人发文占比 0.55%
自引率 0%
平均录取率约50%
平均审稿周期 平均2.3月
版面费 -
偏重研究方向 医学-肿瘤学

期刊高被引文献

LncRNA SNHG5 affects cell proliferation, metastasis and migration of colorectal cancer through regulating miR-132-3p/CREB5
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1537579
KCNQ1OT1/miR-217/ZEB1 feedback loop facilitates cell migration and epithelial-mesenchymal transition in colorectal cancer
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1579959
A regulatory circuit of circ-MTO1/miR-17/QKI-5 inhibits the proliferation of lung adenocarcinoma
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1598762
Research progress of circular RNAs in lung cancer
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1523848
FSTL1 enhances chemoresistance and maintains stemness in breast cancer cells via integrin β3/Wnt signaling under miR-137 regulation
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1529101
Neratinib and entinostat combine to rapidly reduce the expression of K-RAS, N-RAS, Gαq and Gα11 and kill uveal melanoma cells
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1551747
Glycogen synthase kinase-3 beta inhibitors as novel cancer treatments and modulators of antitumor immune responses
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1595283
Upregulation of long non-coding RNA NNT-AS1 promotes osteosarcoma progression by inhibiting the tumor suppressive miR-320a
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1538612
The LncRNA LINC00963 facilitates osteosarcoma proliferation and invasion by suppressing miR-204-3p/FN1 axis
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1598766
LncRNA RMRP silence curbs neonatal neuroblastoma progression by regulating microRNA-206/tachykinin-1 receptor axis via inactivating extracellular signal-regulated kinases
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1550568
EGR1-induced upregulation of lncRNA FOXD2-AS1 promotes the progression of hepatocellular carcinoma via epigenetically silencing DKK1 and activating Wnt/β-catenin signaling pathway
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1595276
MiR-202-5p/PTEN mediates doxorubicin-resistance of breast cancer cells via PI3K/Akt signaling pathway
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1591674
Comprehensive analysis of the long noncoding RNA expression profile and construction of the lncRNA-mRNA co-expression network in colorectal cancer
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1673098
Prior exposure of pancreatic tumors to [sorafenib + vorinostat] enhances the efficacy of an anti-PD-1 antibody
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1507258
Weighted gene co-expression network analysis and prognostic analysis identifies hub genes and the molecular mechanism related to head and neck squamous cell carcinoma
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1564560
LINC01133 promotes the progression of cervical cancer by sponging miR-4784 to up-regulate AHDC1
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1647058
Predictive and prognostic value of PDL1 protein expression in breast cancer patients in neoadjuvant setting
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1583533
CXCR4/TGF-β1 mediated hepatic stellate cells differentiation into carcinoma-associated fibroblasts and promoted liver metastasis of colon cancer
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1685157
Serum metabolite profiling of familial adenomatous polyposis using ultra performance liquid chromatography and tandem mass spectrometry
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1595277
Cancer-associated fibroblasts promote colorectal cancer progression by secreting CLEC3B
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1591122
Photoimmunotherapy for cancer-associated fibroblasts targeting fibroblast activation protein in human esophageal squamous cell carcinoma
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1617566
Low pretreatment lymphocyte/monocyte ratio is associated with the better efficacy of neoadjuvant chemotherapy in breast cancer patients
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1680057
The in cis compound EGFR mutations in Chinese advanced non-small cell lung cancer patients
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1595280
The histone deacetylase inhibitor Suberoylanilide Hydroxamic Acid (SAHA) as a therapeutic agent in rhabdomyosarcoma
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1529093
Visfatin is involved in the cisplatin resistance of osteosarcoma cells via upregulation of Snail and Zeb1
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1591675
PDGFRα expression as a novel therapeutic marker in well-differentiated neuroendocrine tumors
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1529114
Tumor regression after combination of radiation and PD-1 antibody nivolumab treatment in a patient with metastatic mediastinal leiomyosarcoma: a case report
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1537577
Adeno-associated virus 2 mediated gene transfer of vascular endothelial growth factor Trap: a new treatment option for glioma
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1504725
Expression of the SNAI2 transcriptional repressor is regulated by C16-ceramide
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1579962
Beta 2-microglobulin regulates amyloid precursor-like protein 2 expression and the migration of pancreatic cancer cells
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1580414
Discovery and mechanisms of host defense to oncogenesis: targeting the β-defensin-1 peptide as a natural tumor inhibitor
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1564564
GSK343 induces programmed cell death through the inhibition of EZH2 and FBP1 in osteosarcoma cells
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1680061
De novo MET amplification promotes intrinsic resistance to first-generation EGFR tyrosine kinase inhibitors
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1617568
Sodium chloride (NaCl) potentiates digoxin-induced anti-tumor activity in small cell lung cancer
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1504723
Endometriosis-associated ovarian cancer is a single entity with distinct clinicopathological characteristics
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1595278
Schedule-dependent potentiation of chemotherapy drugs by the hypoxia-activated prodrug SN30000
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1617570
2-Methoxy-5((3,4,5-trimethosyphenyl)seleninyl) phenol reverses EGF-induced cell migration and invasion through down-regulation of MDM2 in breast cancer cell lines
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1537578
Montelukast enhances cytocidal effects of carfilzomib in multiple myeloma by inhibiting mTOR pathway
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1529112
SEMA4D under the posttranscriptional regulation of HuR and miR-4319 boosts cancer progression in esophageal squamous cell carcinoma
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1669996
BMSC-derived leptin and IGFBP2 promote erlotinib resistance in lung adenocarcinoma cells through IGF-1R activation in hypoxic environment
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1665952
Combined α-programmed death-1 monoclonal antibody blockade and fractionated radiation therapy reduces tumor growth in mouse EL4 lymphoma
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1550569
Unexpected favorable outcome to etoposide and cisplatin in a small cell lung cancer transformed patient: a case report
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1617561
Correction notice
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1699718
Discovery platform for inhibitors of IgH gene enhancer activity
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1538615
Successful treatment of a BRAF V600E-mutant extracranial metastatic anaplastic oligoastrocytoma with vemurafenib and everolimus
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2018.1529115
Discovery and characterization of a novel highly potent and selective type II native and drug-resistant V299L mutant BCR-ABL inhibitor (CHMFL-ABL-039) for Chronic Myeloid Leukemia (CML)
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1579958
Two dichloric compounds inhibit in vivo U87 xenograft tumor growth
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1632131
Comparison of 21-gene assay and St.Gallen International Expert Consensus in the treatment decision for patients with early invasive breast cancers
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1669994
A case of primary pulmonary atypical carcinoid with EML4-ALK rearrangement
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1665957
Meningeal metastasis of a malignant peritoneal mesothelioma: A case report and literature review
来源期刊:Cancer Biology & TherapyDOI:10.1080/15384047.2019.1647053

质量指标占比

研究类文章占比 OA被引用占比 撤稿占比 出版后修正文章占比
83.64%100%-2.7%

相关指数

影响因子
影响因子
年发文量
自引率

预警情况

查看说明
时间 预警情况
2026年03月发布的新锐学术版不在预警名单中
2025年03月发布的2025版不在预警名单中
2024年02月发布的2024版不在预警名单中
2023年01月发布的2023版不在预警名单中
2021年12月发布的2021版不在预警名单中
2020年12月发布的2020版不在预警名单中
*来源:中科院《 国际期刊预警名单》

JCR分区

WOS分区等级:1区
版本 按学科 分区
WOS期刊SCI分区
WOS期刊SCI分区
WOS期刊SCI分区是指SCI官方(Web of Science)为每个学科内的期刊按照IF数值排 序,将期刊按照四等分的方法划分的Q1-Q4等级,Q1代表质量最高,即常说的1区期刊。
(2024-2025年最新版)
ONCOLOGY
Q1

中科院分区

查看说明
版本 大类学科 小类学科 Top期刊 综述期刊
2026年3月发布
(新锐分区)
医学2区
ONCOLOGY 肿瘤学
3区
N/A
2025年3月升级版
医学2区
ONCOLOGY 肿瘤学
3区
2023年12月旧的升级版
医学4区
ONCOLOGY 肿瘤学
4区

CiteScore

查看说明
CiteScore SJR SNIP 学科 分区 排名
6.20
1.202
0.723
大类:Medicine 小类:Oncology
大类:Medicine 小类:Pharmacology
大类:Medicine 小类:Cancer Research
大类:Medicine 小类:Molecular Medicine
Q2
Q2
Q2
Q2
107 / 415
103 / 321
88 / 233
80 / 177

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