Literature DB >> 30309504

Tumor-targeting Salmonella typhimurium A1-R overcomes partial carboplatinum-resistance of a cancer of unknown primary (CUP).

Kentaro Miyake1, Tasuku Kiyuna2, Masuyo Miyake1, Ming Zhao3, Sintawat Wangsiricharoen3, Kei Kawaguchi2, Zhiying Zhang2, Takashi Higuchi2, Sahar Razmjooei3, Yunfeng Li4, Scott D Nelson4, Tara Russell5, Arun Singh6, Takashi Murakami7, Yukihiko Hiroshima7, Masashi Momiyama7, Ryusei Matsuyama7, Takashi Chishima7, Shree Ram Singh8, Sant P Chawla9, Fritz C Eilber10, Itaru Endo11, Robert M Hoffman12.   

Abstract

Cancer of unknown primary (CUP) is metastatic disease without a known primary and therefore very difficult to identify effective therapy. Previously, we demonstrated partial efficacy of Salmonella typhimurium A1-R (S. typhimurium A1-R) alone and carboplatinum alone (CAR) on a CUP patient tumor in the patient-derived xenograft (PDOX) model. The aim of the present study was to investigate the efficacy of S. typhimurium A1-R combined with CAR on the CUP PDOX model. The CUP tumors were implanted orthotopically into the left supraclavicular fossa of nude mice to match the site from which they were resected from the patient. CUP PDOX models were divided randomly into the following 4 groups after the tumor volume reached 100 mm3: G1: untreated group; G2: CAR (30 mg/kg, i.p., weekly, 2 weeks); G3: S. typhimurium A1-R (5x107 CFU/body, i.v., weekly, 2 weeks).; G4: S. typhimurium A1-R combined with CAR (S. typhimurium A1-R; 5x107 CFU/body, i.v., weekly, 2 weeks; CAR, 30 mg/kg, i.p., weekly, 2 weeks). Each group comprised 7 mice. All mice were sacrificed on day 15. Tumor volume and body weight were measured twice a week. S. typhimurium A1-R and CAR moderately inhibited tumor growth compared to the untreated group on day 15 (P < 0.001 and P < 0.001, respectively). S. typhimurium A1-R combined with CAR inhibited the tumor growth significantly more compared to S. typhimurium A1-R monotherapy or CAR monotherapy on day 15 (P = 0.004 and P = 0.001, respectively). The present report demonstrates that S. typhimurium A1-R can increase the efficacy of a standard drug used for CUP in a PDOX model. Published by Elsevier Ltd.

Entities:  

Keywords:  CUP; Cancer of unknown primary; Carboplatinum efficacy; Nude mice; PDOX; Patient-derived orthotopic xenograft; Salmonella typhimurium A1-R

Mesh:

Substances:

Year:  2018        PMID: 30309504     DOI: 10.1016/j.tice.2018.09.001

Source DB:  PubMed          Journal:  Tissue Cell        ISSN: 0040-8166            Impact factor:   2.466


  2 in total

Review 1.  Salmonella-Mediated Cancer Therapy: An Innovative Therapeutic Strategy.

Authors:  Ze Mi; Zhi-Chao Feng; Cheng Li; Xiao Yang; Meng-Tian Ma; Peng-Fei Rong
Journal:  J Cancer       Date:  2019-08-20       Impact factor: 4.207

2.  An mTOR and VEGFR inhibitor combination arrests a doxorubicin resistant lung metastatic osteosarcoma in a PDOX mouse model.

Authors:  Hiromichi Oshiro; Yasunori Tome; Kentaro Miyake; Takashi Higuchi; Norihiko Sugisawa; Fuminori Kanaya; Kotaro Nishida; Robert M Hoffman
Journal:  Sci Rep       Date:  2021-04-21       Impact factor: 4.379

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.