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Molecular Cancer Therapeutics

Molecular Cancer Therapeutics is a leading scientific journal that focuses on the latest advancements in cancer research and therapeutic strategies at the molecular level. It publishes cutting-edge studies on targeted therapies, drug development, and personalized medicine, providing valuable insights into the molecular mechanisms of cancer and potential treatments. This journal serves as a vital resource for researchers, clinicians, and pharmaceutical professionals working towards improving cancer treatment outcomes.

Details
Abbr. Mol Cancer Ther
Start 2001
End Continuing
Frequency Monthly
p-ISSN 1535-7163
e-ISSN 1538-8514
Country United States
Language English
Metrics
h-index / Ranks: 730 199
SJR / Ranks: 960 2270
CiteScore / Ranks: 1344 10.30
JIF / Ranks: 1231 5.7
Recent Articles
1.
Matar S, Skah S, Diomande L, Buss T, Hagland H, Yadav A, et al.
Mol Cancer Ther . 2025 Mar; PMID: 40084615
Therapeutic anti-CD47 monoclonal antibodies (mAbs) are designed to block the CD47-SIRPα checkpoint and promote immune-mediated recognition and elimination of cancer cells. However, current anti-CD47 mAbs have limitations, including off-tumor toxicity...
2.
Mistry H, Hodson D, Battula S, Schmidt M, Tighe R, Kaufman H, et al.
Mol Cancer Ther . 2025 Mar; PMID: 40079372
Interleukin-12 (IL-12) mediates innate and adaptive immune responses and has demonstrated therapeutic anti-tumor activity but clinical development has been hindered by a narrow therapeutic window. We generated a novel IL-12...
3.
Dong L, Zhang S, Wuri Q, Qu X, Zhang K, Cai Z, et al.
Mol Cancer Ther . 2025 Mar; :OF1-OF11. PMID: 40066767
Mounting evidence suggests that immunotherapies are promising strategies for fighting against cancers. However, the immunosuppressive tumor microenvironment (TME), insufficient lymphocytic infiltration, and poor immunogenicity hamper the broader implementation of immunotherapies....
4.
Cudmore A, Rodriguez G, Maranda V, Boroujeni S, Murshed H, Macdonald E, et al.
Mol Cancer Ther . 2025 Mar; PMID: 40062380
Epithelial Ovarian Cancer (EOC) is the most lethal gynecologic cancer and those affected are in urgent need of new therapeutic strategies. Standard treatment is surgery followed by taxane- and platinum-based...
5.
Zhang S, Xue H, Wong N, Doerksen T, Ban F, Anderson S, et al.
Mol Cancer Ther . 2025 Mar; PMID: 40062378
Nucleobase analogue (NBA) drugs, such as 5-fluorouracil (5-FU), are effective chemotherapeutics, but their clinical use is limited by severe side effects. Compelling evidence suggests that the use of S-methyl-5'-thioadenosine (MTA)...
6.
Yamaguchi A, Yamazaki C, Anami Y, Ha S, Xiong W, Ta R, et al.
Mol Cancer Ther . 2025 Mar; PMID: 40051166
To explore the potential of site-selectively radiolabeled antibody-drug conjugates (ADCs) against solid tumors, we constructed and evaluated radiolabeled ADCs equipped with lutetium-177 (177Lu) and a membrane permeable antimitotic agent. Site-selective...
7.
Gu H, Qi S, Chen J, Wu H, Xu J, Feng Y
Mol Cancer Ther . 2025 Mar; PMID: 40036166
Ovarian cancer (OC) is a common malignant tumor in the female reproductive system. Paclitaxel resistance is the primary cause of treatment failure in patients with OC. Therefore, elucidating the mechanisms...
8.
Georgiev T, Puglioli S, Principi L, Gilardoni E, Pellegrino C, Bassi G, et al.
Mol Cancer Ther . 2025 Mar; PMID: 40034039
Prostate Specific Membrane Antigen (PSMA) is a transmembrane glycoprotein that is over-expressed on the surface of cancerous prostate cells both in primary tumors and in metastases. Small organic ligands targeting...
9.
Esdar C, LInde N, Blum A, Schieferstein H, Drechsler C, Sherbetjian E, et al.
Mol Cancer Ther . 2025 Feb; PMID: 40018846
Primary activating mutations in KIT (exons 9/11) are key driver alterations in about 80% of gastrointestinal stromal tumors (GIST). Imatinib, a small molecule tyrosine kinase inhibitor, is used successfully as...
10.
Mattson Cypert B, Menard K, Chu G, McDevitt T, Verona R, Rupnow B, et al.
Mol Cancer Ther . 2025 Feb; PMID: 40008870
Prostate cancer is considered immunologically "cold", with low mutational burden, tumor-infiltrating immune cells, and PD-L1 levels, culminating in poor response to immune checkpoint therapies. Bispecific CD3 redirection antibodies can elicit...