Effect of PTEN mRNA expression level in granulosa cells on follicular fluid hormone secretion in infertile patients with polycystic ovary syndrome

Jianfeng YAO, Peiya WU, Liying CHEN, Yanting WANG, Youxia LING, Xiaoyan CHEN, Wanzhen CHEN, Ping TAO, Rongfu HUANG, Youzhu LI

PDF(627 KB)
PDF(627 KB)
J Jilin Univ Med Ed ›› 2025, Vol. 51 ›› Issue (1) : 164-171. DOI: 10.13481/j.1671-587X.20250120
Research in clinical medicine

Effect of PTEN mRNA expression level in granulosa cells on follicular fluid hormone secretion in infertile patients with polycystic ovary syndrome

Author information +
History +

Abstract

Objective To detect the levels of sex hormones and insulin in follicular fluid(FF) and the expression level of phosphatase and tensin homolog deleted on chromosome ten(PTEN) in granulosa cells in the infertile patients with polycystic ovary syndrome(PCOS), and to preliminarily explain the correlations between the insulin level and the expression level of PTEN mRNA. Methods Seventy infertile patients were selected as the subjects and divided into PCOS group and control group (tubal obstruction or infertility due to male factors) according to infertility factors. All patients received in vitro fertilization-embryo transfer(IVF-ET) treatment. FF and ovarian granulosa cells were collected on the day of ovulation. The expression levels of PTEN mRNA in ovarian granulosa cells of the patients in two groups were detected by real-time fluorescence quantitative PCR(RT-qPCR) method. The levels of sex hormone and insulin in FF were measured by electrochemiluminescence. The correlations of the PTEN mRNA expression level in ovarian granulosa cells and testosterone(T) in FF with the level of insulin in FF were analyzed by Spearman correlation analysis method. Results There were no significant differences in age, infertility years, body mass index (BMI), basic sex hormone, total dose of gonadotropin(Gn) and days of ovulation induction in two groups(P>0.05). Compared with control group, the anti-Mullerian hormone(AMH) and antral follicle counting(AFC) of the patients in PCOS group were significantly increased(P<0.05). The RT-qPCR results showed that the PTEN mRNA expression level in ovarian granulosa cells of the patients in the PCOS group was higher than that in control group(P<0.001). The electrochemiluminescence results showed that the levels of T and insulin in FF of the patients in PCOS group were higher than those in control group(P<0.05), whereas the estrogen and progesterone levels were lower than those in control group(P<0.05). The Spearman correlation analysis showed that that T level in FF was positively correlated with the insulin level of the patients in PCOS group(r=0.577, P<0.001), and the PTEN mRNA expression level in ovarian granulosa cells was positively correlated with the insulin levels in FF (r=0.616, P<0.001); in control group, there was no correlation between T level and insulin level in FF(r=0.266, P=0.123), and there was no correlation between the expression level ofPTEN mRNA in granulosa cells and the insulin level in FF in control group (r=-0.214, P=0.216). Conclusion The high expression of PTEN in granulosa cells of the infertile patients with PCOS may be related to the local hyperinsulin level in the ovary, and PTEN participates in the occurrence and development of PCOS.

Key words

Polycystic ovary syndrome / Follicular fluid / Insulin / Granulosa cell / Phosphatase and tensin homolog deleted on chromosome 10

Cite this article

Download Citations
Jianfeng YAO , Peiya WU , Liying CHEN , et al . Effect of PTEN mRNA expression level in granulosa cells on follicular fluid hormone secretion in infertile patients with polycystic ovary syndrome. Journal of Jilin University(Medicine Edition). 2025, 51(1): 164-171 https://doi.org/10.13481/j.1671-587X.20250120

References

1
ARMANINI D BOSCARO M BORDIN L, et al. Controversies in the pathogenesis, diagnosis and treatment of PCOS: focus on insulin resistance, inflammation, and hyperandrogenism[J]. Int J Mol Sci202223(8): 4110.
2
HERMAN R SIKONJA J JENSTERLE M, et al. Insulin metabolism in polycystic ovary syndrome: secretion, signaling, and clearance[J]. Int J Mol Sci202324(4):3140.
3
WANG K X LI Y H. Signaling pathways and targeted therapeutic strategies for polycystic ovary syndrome[J].Front Endocrinol202314:1191759.
4
LEE Y R CHEN M PANDOLFI P P. The functions and regulation of the PTEN tumour suppressor: new modes and prospects[J]. Nat Rev Mol Cell Biol201819(9): 547-562.
5
HU C F ZHAO X Y CUI C, et al. miRNA-29-3p targets PTEN to regulate follicular development through the PI3K/Akt/mTOR signaling pathway[J]. Theriogenology2024214:173-181.
6
RAMASUBBU K DEVI RAJESWARI V. Impairment of insulin signaling pathway PI3K/Akt/mTOR and insulin resistance induced AGEs on diabetes mellitus and neurodegenerative diseases: a perspective review[J]. Mol Cell Biochem2023478(6):1307-1324.
7
LI Y Z DI CRISTOFANO A, WOO M. Metabolic role of PTEN in insulin signaling and resistance[J]. Cold Spring Harb Perspect Med202010(8): a036137.
8
ROTTERDAM ESHRE/ASRM-SPONSORED PCOS CONSENSUS WORKSHOP GROUP. Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS)[J]. Hum Reprod200419(1): 41-47.
9
YAO J F HUANG R F LI M, et al. PTEN expression in human granulosa cells is associated with ovarian responses and clinical outcomes in IVF[J]. Reprod Sci202128(7): 1910-1921.
10
MYERS S H RUSSO M DINICOLA S, et al. Questioning PCOS phenotypes for reclassification and tailored therapy[J]. Trends Endocrinol Metab202334(11):694-703.
11
WANG J WU D C GUO H, et al. Hyperandrogenemia and insulin resistance: the chief culprit of polycystic ovary syndrome[J]. Life Sci2019236: 116940.
12
ZHANG S TU H Y ZHU J M, et al. Dendrobium Nobile Lindl. polysaccharides improve follicular development in PCOS rats[J]. Int J Biol Macromol2020149: 826-834.
13
XU Y L QIAO J. Association of insulin resistance and elevated androgen levels with polycystic ovarian syndrome (PCOS): a review of literature[J]. J Health Eng20222022: 9240569.
14
吴效科. 多囊卵巢综合征可能是原发性卵泡病[J].中国实用妇科与产科杂志200723(9): 660-663.
15
ZHU Q L YAO Y XU L Z, et al. Elevated SAA1 promotes the development of insulin resistance in ovarian granulosa cells in polycystic ovary syndrome[J]. Reprod Biol Endocrinol202220(1): 4.
16
CHAI C S WU H H ABUETABH Y, et al. Regulation of the tumor suppressor PTEN in triple-negative breast cancer[J]. Cancer Lett2022527: 41-48.
17
YAO J F LI M LIN L Q, et al. PTEN expression in human cumulus cells is associated with embryo development competence[J]. Zygote202230(5): 611-618.
18
MACUT D BJEKIĆ-MACUT J RAHELIĆ D, et al. Insulin and the polycystic ovary syndrome[J]. Diabetes Res Clin Pract2017130: 163-170.
19
YU N ROY S K. Development of primordial and prenatal follicles from undifferentiated somatic cells and oocytes in the hamster prenatal ovary in vitro: effect of insulin[J]. Biol Reprod199961(6): 1558-1567.
20
靳 镭, 聂 睿. 高胰岛素血症与多囊卵巢综合征大鼠排卵障碍的相关性研究[J]. 生殖医学杂志200817(4): 276-280.
21
GOODARZI M O DUMESIC D A CHAZENBALK G, et al. Polycystic ovary syndrome: etiology, pathogenesis and diagnosis[J]. Nat Rev Endocrinol20117(4): 219-231.
22
LI A D ZHANG L JIANG J J, et al. Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels[J]. J Biomed Res201732(3): 208-214.
23
CRESPO-MASIP M PÉREZ-GÓMEZ A GUZMÁN C, et al. PTEN deletion in adult mice induces hypoinsulinemia with concomitant low glucose levels[J]. Front Endocrinol202213: 850214.
24
HUANG X J LIU G H GUO J, et al. The PI3K/AKT pathway in obesity and type 2 diabetes[J]. Int J Biol Sci201814(11): 1483-1496.
25
MOGHETTI P TOSI F. Insulin resistance and PCOS: chicken or egg?[J]. J Endocrinol Invest202144(2): 233-244.

姚建凤和黄荣富参与选题及论文撰写,吴培雅和作者贡献声明:

陈丽影参与论文选题、临床数据及实验标本收集,王燕婷和凌幼霞参与实验操作过程,陈晓燕、陈婉真和陶萍参与数据的统计学分析,李友筑参与论文撰写和论文修改。

RIGHTS & PERMISSIONS

© Editorial Board of Journal of Jilin University(Medicine Edition). Open access under CC BY-NC-ND license.

Comments

PDF(627 KB)

Accesses

Citation

Detail

Sections
Recommended

/