<italic style="font-style: italic">Lactobacilli</italic> culture supernatant enhances sensitivity of triple-negative breast cancer cells to cisplatin <italic style="font-style: italic">via</italic> down-regulation of Piwil2

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Lactobacilli culture supernatant enhances sensitivity of triple-negative breast cancer cells to cisplatin via down-regulation of Piwil2

Basic Medicine | 更新时间：2026-01-09

- Lactobacilli culture supernatant enhances sensitivity of triple-negative breast cancer cells to cisplatin via down-regulation of Piwil2
- Journal of Third Military Medical University Vol. 39, Issue 12, Pages: 1200-1205(2017)
- 作者机构：
  
  1.400037 重庆，第三军医大学新桥医院普通外科
  2.400038 重庆，第三军医大学基础医学部生物化学与分子生物学教研室
- 作者简介：
- 基金信息：
  
  the General Program of National Natural Science Foundation of China(31571459);the General Program of National Natural Science Foundation of China(81272908)
- DOI：10.16016/j.1000-5404.201703052
  CLC： R378.992;R737.9;R979.12
- Received：09 March 2017，
  
  Revised：2017-03-26，
  
  Published：30 June 2017
- 稿件说明：
移动端阅览
Tao Li, Xiaogan Ma, Bin Chen, et al. Lactobacilli culture supernatant enhances sensitivity of triple-negative breast cancer cells to cisplatin via down-regulation of Piwil2[J]. Journal of Third Military Medical University, 2017, 39(12): 1200-1205.
DOI：

Tao Li, Xiaogan Ma, Bin Chen, et al. Lactobacilli culture supernatant enhances sensitivity of triple-negative breast cancer cells to cisplatin via down-regulation of Piwil2[J]. Journal of Third Military Medical University, 2017, 39(12): 1200-1205. DOI： 10.16016/j.1000-5404.201703052.

摘要

目的

2

探讨乳酸菌培养上清液(

lactobacilli

supernatants，LS)处理乳腺癌细胞对顺铂(cisplatin，DDP)敏感性的影响及其机制。

方法

2

采用CCK-8和Western blot检测不同浓度DDP(0、1、2、3、4、5 μg/mL)和LS(体积分数分别为1%、5%、10%、20%)对三阴性乳腺癌细胞MDA-MB-231增殖和Piwil2基因表达的影响；瞬时转染Piwil2 siRNA沉默MDA-MB-231细胞中Piwil2基因表达，Western blot检测其沉默效果，CCK-8检测Piwil2基因沉默后对MDA-MB-231细胞增殖的影响；2 μg/mL DDP联合不同浓度LS(体积分数分别为1%、5%、10%、20%)作用MDA-MB-231细胞，观察细胞增殖抑制效应和Piwil2蛋白表达的改变。

结果

2

高浓度DDP(≥3 μg/mL)可抑制MDA-MB-231细胞的增殖(

P

<

0.05)，而低浓度DDP(≤2 μg/mL)不能有效抑制细胞增殖；DDP以剂量依赖性方式上调Piwil2蛋白的表达；siRNA沉默Piwil2表达可恢复2 μg/mL DDP对细胞增殖的抑制。与对照组(乳酸菌培养基，MRS)比较，LS以剂量依赖性方式下调Piwil2蛋白的表达，但并不影响细胞的增殖；与单用2 μg/mL DDP比较，2 μg/mL DDP联合20% LS处理可显著下调Piwil2蛋白的表达并抑制细胞增殖(

P

<

0.05)。

结论

2

三阴性乳腺癌细胞中Piwil2的高表达可导致细胞对顺铂敏感性的降低，乳酸菌培养上清液可通过下调Piwil2基因的表达增强三阴性乳腺癌细胞对顺铂的敏感性。

Abstract

Objective

2

To assess the effect of

Lactobacilli

culture supernatant (LS) on the sensitivity of breast cancer cell line MDA-MB-231 to cisplatin(DDP) and investigate its underlying mechanism.

Methods

2

CCK8 assay and Western blotting were used to observe the proliferation and the expression of Piwil2

respectively

in triple-negative MDA-MB-231 cells treated with DDP(0

1

2

3

4 and 5 μg/mL) or LS (1%

5%

10% and 20%

V/V) for 24 h. In MDA-MB-231 cells transiently transfected with Piwil2 siRNA to silence the expression of Piwil2

the cell proliferation was detected with CCK8 assay.The expression of Piwil2 and cell proliferation were also observed in the MDA-MB-231 cells treated with 2 μg/mL DDP combined with LS (1%

5%

10% and 20%

V/V) for 24 h.

Results

2

DDP at high doses(≥3 μg/mL)

but not at lower doses(≤2 μg/mL)

effectively inhibited the proliferation of MDA-MB-231 cells(

P

<

0.05). Western blotting showed that DDP up-regulated the expression of Piwil2 in a dose-dependent manner. siRNA-mediated Piwil2 silencing restored the inhibitory effect of 2 μg/mL DDP on the proliferation of MDA-MB-231 cells. Compared with the culture medium for

Lactobacilli

that did not contain

Lactobacilli

(vehicle)

LS dose-dependently down-regulated the expression of Piwil2 without affecting the cell proliferation. Compared with DDP(2 μg/mL) treatment alone

DDP(2 μg/mL) combined with LS(20%) significantly down-regulated Piw

il2 expression and also inhibited the proliferation of MDA-MB-231 cells (

P

<

0.05).

Conclusion

2

High expression of Piwil2 may cause lowered sensitivity of tumor cells to DDP

and LS can enhance the sensitivity of MDA-MB-231 cells to DDP by down regulating Piwil2.

关键词

Keywords

references

Siegel R L, Miller K D, Jemal A. Cancer statistics, 2016[J]. CA Cancer J Clin, 2016, 66(1): 7-30. DOI:10.3322/caac.21332.

Jiao Q, Wu A, Shao G, et al . The latest progress in research on triple negative breast cancer (TNBC): risk factors, possible therapeutic targets and prognostic markers[J ] .J Thorac Dis, 2014, 6(9): 1329-1335. DOI:10.3978/j.issn.2072-1439.2014.08.13.

Gamallat Y, Meyiah A, Kuugbee E D, et al . Lactobacillus rhamnosus induced epithelial cell apoptosis, ameliorates inflammation and prevents colon cancer development in an animal model[J ] . Biomed Pharmacother, 2016, 83: 536-541. DOI:10.1016/j.biopha.2016.07.001.

Nouri Z, Karami F, Neyazi N, et al . Dual anti-metastatic and anti-proliferative activity assessment of two probiotics on heLa and HT-29 cell lines[J ] . Cell J, 2016, 18(2): 127-134.

Fukui M, Fujino T, Tsutsui K, et al . The tumor-preventing effect ofamixture of several lactic acid bacteria on 1, 2-dimethylhydrazine-induced colon carcinogenesis in mice[J ] . Oncol Rep, 2001, 8(5): 1073-1078. DOI:10.3892/or.8.5.1073.

Azam R, Ghafouri-Fard S, Tabrizi M, et al . Lactobacillus acidophilus and Lactobacillus crispatus culture supernatants downregulate expression of cancer-testis genes in the MDA-MB-231 cell line[J ] . Asian Pac J Cancer Prev, 2014, 15(10): 4255-4259. DOI:10.7314/apjcp.2014.15.10.4255.

Chen X, He C, Han D, et al . The predictive value of Ki-67 before neoadjuvant chemotherapy for breast cancer:asystematic review and meta-analysis[J ] . Future Oncol, 2017, 13(9): 843-857. DOI:10.2217/fon-2016-0420.

Medina-Aguilar R, Pérez-Plasencia C, Gariglio P, et al . DNA methylation data for identification of epigenetic targets of resveratrol in triple negative breast cancer cells[J ] . Data in Brief, 2017, 11: 169-182. DOI:10.1016/j.dib.2017.02.006.

Scanlan M J, Gure A O, Jungbluth A A, et al . Cancer/testis antigens: an expanding family of targets for cancer immunotherapy[J ] . Immunol Rev, 2002, 188: 22-32.

Liu J J, Shen R, Chen L, et al . Piwil2 is expressed in various stages of breast cancers and has the potential to be used asanovel biomarker[J ] . Int J Clin Exp Pathol, 2010, 3(4): 328-337.

[Torkashvand S, Damavandi Z, Mirzaei B, et al . Decreased expression of bioinformatically predicted piwil2-targetting microRNAs, miR-1267 and miR-2276 in breast cancer[J ] . Arch Iran Med, 2016, 19(6): 420-425. DOI: 0161906/AIM.009 http://dx.doi.org/0161906/AIM.009 ..

Manakov S A, Pezic D, Marinov G K, et al . MIWI2 and MILI have differential effects on piRNA biogenesis and DNA methylation[J ] . Cell Rep, 2015, 12(8): 1234-1243. DOI: 10.1016/j.celrep.2015.07.036.

Amable L. Cisplatin resistance and opportunities for precision medicine[J]. Pharmacol Res, 2016, 106: 27-36. DOI:10.1016/j.phrs.2016.01.001.

程敏. 沉默Piwil2增强子宫颈癌细胞对顺铂敏感性的机制研究[D]. 合肥: 安徽医科大学, 2013.

Chen M.The mechanisms research of silence Piwil2 enhanced cervical cancer cell sensitivity to cisplatin[D]. Hefei: Anhui Medical Univercity, 2013.

Kim Y, Oh S, Yun H S, et al . Cell-bound exopolysaccharide from probiotic bacteria induces autophagic cell death of tumour cells[J ] . Lett Appl Microbiol, 2010, 51(2): 123-130. DOI: 10.1111/j.1472-765X.2010.02859.x.

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