Home  |  About JAPTR |  Editorial board  |  Search |  Ahead of print  |  Current issue  |  Archives |  Submit article  |  Instructions  |  Subscribe  |  Advertise  |  Contacts  |Login 
Users Online: 184   Home Print this page Email this page Small font sizeDefault font sizeIncrease font size

Year : 2010  |  Volume : 1  |  Issue : 2  |  Page : 109-126 Table of Contents     

Various types and management of breast cancer: An overview

1 School of Pharmaceutical Sciences, Jaipur National University, Jaipur, Rajasthan, India
2 Maharishi Arvind Institute of Pharmacy, Jaipur, Rajasthan, India
3 LBS College of Pharmacy, Tilak Nagar, Jaipur, Rajasthan, India

Date of Submission29-Mar-2010
Date of Decision19-May-2010
Date of Acceptance05-Jun-2010
Date of Web Publication2-Nov-2010

Correspondence Address:
Ganesh N Sharma
School of Pharmaceutical Sciences, Jaipur National University, Jaipur, Rajasthan
Login to access the Email id

Source of Support: None, Conflict of Interest: None

PMID: 22247839

Rights and PermissionsRights and Permissions

Now days, breast cancer is the most frequently diagnosed life-threatening cancer in women and the leading cause of cancer death among women. Since last two decades, researches related to the breast cancer has lead to extraordinary progress in our understanding of the disease, resulting in more efficient and less toxic treatments. Increased public awareness and improved screening have led to earlier diagnosis at stages amenable to complete surgical resection and curative therapies. Consequently, survival rates for breast cancer have improved significantly, particularly in younger women. This article addresses the types, causes, clinical symptoms and various approach both non- drug (such as surgery and radiation) and drug treatment (including chemotherapy, gene therapy etc.) of breast cancer.

Keywords: Breast Cancer, Tumor, Chemotherapy, Gene Therapy

How to cite this article:
Sharma GN, Dave R, Sanadya J, Sharma P, Sharma KK. Various types and management of breast cancer: An overview. J Adv Pharm Technol Res 2010;1:109-26

How to cite this URL:
Sharma GN, Dave R, Sanadya J, Sharma P, Sharma KK. Various types and management of breast cancer: An overview. J Adv Pharm Technol Res [serial online] 2010 [cited 2023 Feb 9];1:109-26. Available from: https://www.japtr.org/text.asp?2010/1/2/109/72251

   Introduction Top

Breast cancer is the most common cause of cancer in women and the second most common cause of cancer death in women in the U.S.

Breast cancer refers to cancers originating from breast tissue, most commonly from the inner lining of milk ducts or the lobules that supply the ducts with milk.

Worldwide, breast cancer comprises 10.4% of all cancer incidences among women, making it the second most common type of non-skin cancer (after lung cancer) and the fifth most common cause of cancer death. In 2004, breast cancer caused 519,000 deaths worldwide (7% of cancer deaths; almost 1% of all deaths). Breast cancer is about 100 times more common in women than in men, although males tend to have poorer outcomes due to delays in diagnosis.

Cancer cells are very similar to cells of the organism from which they originated and have similar (but not identical) DNA and RNA. This is the eeason why they are not very often detected by thz immunz system, in particular, if it is weakened [1] .

Cancer cells are formed from normal cells due to a modification / mutation of DNA and / or RNA. These modifications / mutations can occur spontaneously ill Law of Thermodynamics - increase of entropy) or they may be induced by other factors such as; nuclear radiation, electromagnetic radiation (microwaves, X-rays, Gamma-rays, Ultraviolet-rays etc.), viruses, bacteria and fungi, parasites (due to tissue inflammation / irritation, heat, chemicals in the air, water and food, mechanical cell-level injury, free radicals, zvolution and ageing of DNA and RNA, etc. All thzse can produce mutations that may start cancer. Cancer can be called therefore "Entropic Disease" since it is associated with the increase of entropy of the organism to the point where the organism cannot correct this itself External intervention is required to allow the organism to return to a stable entropic state [2] .

Cancer develops if the immune system is not working properly and / or the amount of cells produced is too great for the immune system to eliminate [3]. The rate of DNA and RNA mutations can be too high under some conditions such as; unhealthy emironment (due to radiation, chemicals, etc.) [4], poor diet (unhealthy cell environment) [5] , people with genetic predispositions to mutations [6] and people of advanced age (above 80) [7] .

The Cell cycle

In cancerous cells, thz process of cell division is disrupted and unregulated, resulting in cell proliferation and tumor growth. The normal cell cycle is as represented in [Figure 1].
Figure 1: Stages of normal cell cycle [8]

Click here to view

   Breast Cancer Top

Usually, cancer is named after the body part in which it originated; thus, breast cancer refers to the erratic growth and proliferation of cells that originate in the breast tissue [9] .

The breast is composed of two main types of tissues i.e., glandular tissues and stromal (supporting) tissues. Glandular tissues house the milk­producing glands (lobules) and the ducts (the milk passages) while stromal tissues include fatty and fibrous connective tissues of the breast. The breast is also made up of lymphatic tissue-immune system tissue that removes cellular fluids and waste [10] .

There are several types of tumors that may develop within different areas of the breast. Most tumors are the result of benign (non-cancerous) changes within the breast. For example, fibrocystic change is a non-cancerous condition in which women develop cysts (accumulated packets of fluid), fibrosis (formation of scar-like connective tissue), lumpiness, and areas of thickening, tenderness, or breast pain [11] .

Most breast cancers begin in the cells that line the ducts (ductal cancers). Some begin in the cells that line the lobules (lobular cancers), while a small number start in the other tissues [12].[Figure 2]
Figure 2: Structure of breast

Click here to view

   Types of Breast Cancer Top

According to site

Non-Invasive Breast Cancer cells that are confined to the ducts and do not invade surrounding fatty and connective tissues of the breast. Ductal carcinoma in situ (DCIS) is the most common form of non-invasive breast cancer (90%). Lobular carcinoma in situ (LCIS) is less common and considered a marker for increased breast cancer risk.

Invasive Breast Cancer cells that break through the duct and lobular wall and invade the surrounding fatty and connective tissues of the breast. Oancer can be invasive without being metastatic (spreading) to the lymph nodes or other organs [13] .

Frequently occurring Breast cancer

Lobular carcinoma in situ
(LCIS, lobular neoplasia): The term, "in situ," refers to cancer that has not spread past the area where it initially developed. LCIS is a sharp increase in the number of cells within the milk glands (lobules) of the breast.

Ductal carcinoma in situ (DCIS): DCIS, the most common type of non­invasive breast cancer, is confined to the ducts of the breast. For example, ductal come docarcinoma.[Figure 3]
Figure 3: Typical Structure associated with ductal carcinoma

Click here to view

Infiltrating lobular carcinoma (ILC) ILC is also known as invasive lobular carcinoma. ILC begins in the milk glands (lobules) of the breast, but often spreads (metastatizes) to other regions of the body. ILC accounts for 10% to 15% of breastt cancers.

Infiltrating ductal carcinoma (IDC): IDC is also known as invasive ductal carcinoma. IDC begins in the milk ducts of the breast and penetrates the wall of the duct, invading the fatty tissue of the breast and possibly other regions of the body. IDC is the most common type of breast cancer, accounting for 80% of breast cancer diagnoses [14],[15] .

Less commonly occurring Breast cancer

Medullary carcinoma:
Medullary carcinoma is an invasive breast cancer that forms a distinct boundary between tumor tissue and normal tissue. Only 5% of breast cancers are medullary carcinoma.

Mutinous carcinoma: Also called colloid carcinoma, mutinous carcinoma is a rare breast cancer formed by the mucus-producing cancer cells. Women with mutinous carcinoma generally have a better prognosis than women with more common types of invasive carcinoma.

Tubular carcinoma.: Tubular carcinomas are a special type of infiltrating - (invasive) breast carcinoma. Women with tubular carcinoma generally have a better prognosis than women with more common types of invasive carcinoma. Tubular carcinomas account for around 2% of breast cancer diagnoses.

Inflammatory breast cancer Inflammatory breast cancer is the appearance of inflamed breasts (red and warm) with dimples and/or thick ridges caused by cancer cells blocking lymph vessels or channels in the skin over the breast. Though inflammatory breast cancer is rare (accounting for only 1% of breast cancers), it is extremely fast­-growing.

Paget's disease of the nipple

A rare form of breast cancer that begins in the milk ducts and spreads to the skin of the nipple and areola, Paget's disease of the nipple only accounts for about 1% of breast cancers.

Phylloides tumor

Phylloides tumors (also spelled "phyllodes") are can be either benign (non-cancerous) or malignant (cancerous). Phylloides tumors develop in the connective tissues of the breast and may be treated by surgical removal. Phylloides tumors are very rare; less than 10 women die of this type of breast cancer each year in the United States [16],[17],[18] .

   Causes of Breast Cancer Top

A previous history of breast cancer

A woman who has had breast cancer has an increased risk of getting breast cancer in the other breast [19] .

Significant family history

If several members of patient's family have had particular types of cancer, patient may have an increased risk of developing breast cancer [19],[20] .

Genetic causes

Family history has long been known to be a risk factor for breast cancer. Both maternal and paternal relatives are important. The risk is highest if the affected relative developed breast cancer at a young age, had cancer in both breasts, or if she is a close relative. First-degree relatives, (mother, sister, daughter) are most important in estimating risk. Several second-degree relatives (grandmother, aunt) with breast cancer may also increase risk. Breast cancer in a male increases the risk for all his close female relatives. BRCA1 and BRCA2 are abnormal genes that, when inherited, markedly increase the risk of breast cancer to a lifetime risk estimated between 40 and 8S%. Women who have the BRCA1 gene tend to develop breast cancer at an early age [21] .

Hormonal causes

Alteration in harmonol level may precipitate breast cancer. It could be attended by starting and stopping of periods (Menstrual Cycle), Pregnancy in early age, Hormonal replacement therapy, Use of oral pills etc [22] .

Life style and dietary cause

Sedentary life style, high dietary intake of fat obesity particularly in postmenopausal women may cause breast cancer. The use of alcohol is also another one cause of breast cancer. The risk increases with the amount of alcohol consumed. Women who consume two to five alcoholic beverages per day have a risk about one and a half times that of nondrinkers for the development of breast cancer [23],[24] .

Environmental cause

There is known to be a slight increase in risk in ladies who work with low doses of radiation over a long period of time­for example, X-ray technicians [23],[24] .

Sign and symptoms

The classic symptom for breast cancer is a lump found in the breast or armpit. Doing monthly breast self-exam (BSE) is a great way to be familiar with the breasts' texture, cyclical changes, size, and skin condition. The general alerting features of breast cancer are such as swelling or lump (mass) in the breast, swelling in the armpit (lymph nodes), nipple discharge (clear or bloody), pain in the nipple, inverted (retracted) nipple, scaly or pitted skin on nipple, persistent tenderness of the breast, and unusual breast pain or discomfort. In Advanced stage (Metastatic) of disease underarm lymph nodes are present with other symptoms such as bone pain (bone metastases), shortness of breath (lung metastases), drop in appetite (liver metastases), unintentional weight loss (liver metastases), headaches, neurological pain or weakness [25] .

Screening/diagnosis of breast cancer

Breast cancer is usually diagnosed by biopsy of nodule detected by mammogram or by palpitation [26].[Figure 4]
Figure 4: Various approaches for diagnosis of breast cancer [27]

Click here to view

Stages of Breast Cancer

When cancer is diagnosed, a stage is assigned to it, based on how advanced it is. The stage helps doctors determine the most appropriate treatment and the prognosis. Stages of breast cancer may be described generally as in situ (not invasive) or invasive. Stages may be described in detail and designated by a number (0 through IV).[Table 1]
Table 1: Stages of Breast Cancer [28]

Click here to view

Management of Breast Cancer

Following approaches are to be made for the management of breast cancer. They are as follows;


Depending on the stage and type of the tumor, lumpectomy (removal of the lump only), or surgical removal of the entire breast (mastectomy) is performed. Standard practice requires the surgeon to establish that the tissue removed in the operation has margins clear of cancer, indicating that the cancer has been completely excised. If the removed tissue does not have clear margins, further operations to remove more tissue may be necessary. This may sometimes require removal of part of the pectoralis major muscle, which is the main muscle of the anterior chest wall. More recently, the technique of sentinel lymph node (SLN) dissection has become popular, as it requires the removal of far fewer lymph nodes, resulting in fewer side effects. Advances in sentinel lymph node mapping over the past decade have increased the accuracy of detecting sentinel lymph node from 80% using blue dye alone to between 92% and 98% using combined modalities [29],[30] .

Surgery for breast cancer consists of two main options.

In breast-conserving surgery, only the tumor and an area of normal tissue surrounding it are removed. Breast­conserving surgery includes the following:

Lumpectomy: A small amount of surrounding normal tissue is removed. Wide excision: Also called as partial mastectomy in which somewhat larger amount of the surrounding normal tissue is removed

Quadrantectomy: About one fourth of the breast is removed.[Figure 5]
Figure 5: various types of surgery applied for breast cancer

Click here to view

In mastectomy, all breast tissue is removed.

Radiation Therapy

Radiation therapy involves using high­energy X-rays or gamma rays that target a tumor or post surgery tumor site. These radiations are very effective in killing cancer cells that may remain after surgery or recur where the tumor was removed. In addition to this treatment implanted radioactive catheters (brachytherapy), similar to those used in prostate cancer treatment, can be used. However this treatment option has been superseded by electron beam radiotherapy to the breast scar. Radiation therapy for breast cancer is usually performed after surgery and is an integral component of breast-conserving therapy. The dose of radiation must be strong enough to ensure the elimination of cancer cells. Treatments are typically given over a period of five to seven weeks, performed five days a week. Each treatment takes about 15 minutes [31],[32] .

   Chemotherapy Top

Chemotherapy is the use of anti-cancer drugs to treat cancerous cells. Specific treatment for the breast cancer will be based on; overall health, medical history, age (whether menstruation is there or not), type and stage of the cancer, tolerance for specific medications and procedures etc. Chemotherapy treatments are often given in cycles; a treatment for a period of time, followed by a recovery period, then another treatment. Chemotherapy can be given before surgery to shrink the tumor and sometimes make breast conserving surgery possible rather than a mastectomy. Many times, it is given after surgery and may be given every three weeks or every two weeks in a "dose dense" fashion [33],[34] . Commonly used agents in breast cancer chemotherapy are [35] ;

Nanotechnology in breast cancer

The field of nanotechnology has rapidly evolved as evidenced by the fact that there are more than 150 ongoing clinical trials investigating the efficacy of nanotechnology based drug delivery carriers targeting cancer. Various liposomal doxorubicin formulations were developed in an effort to improve the therapeutic index of the conventional doxorubicin chemotherapy while maintaining its anti-tumor activity. For example, the efficacy of three liposomal doxorubicins are currently being used: liposomal daunorubicin (DaunoXome®), liposomal doxorubicin (D-99, Myocet ™ J), and pegylated liposomal doxorubicin (Doxil® marketed and distributed in the U.S. and Caelyx® distributed outside the U.S.). Generally, these agents exhibit efficacies comparable to those of conventional doxorubicin, except with better safety profiles and less cardio toxicity. In addition to liposomal doxorubicin, albumin-bound paclitaxel (Abraxane ®) is another example of an E PR based nanovector application for breast cancer chemotherapy. Paclitaxel is highly hydrophobic and dissolved in cremophor to prevent paclitaxel precipitation. However, cremophor­associated toxicities are severe (hypersensitivity reaction and neurotoxicity) and challenge the application of paclitaxel. Albumin­bound paclitaxel was developed to improve the solubility of paclitaxel [36]. [Table 2], [Table 3]
Table 2: Chemotherapeutic agents used in management of breast cancer

Click here to view
Table 3: Age related approaches to chemotherapy for management of breast cancer

Click here to view

Recent approaches in management of breast cancer

Gene Therapy

It is generally accepted that cancer arises because of an accumulation of multiple molecular genetic defects that culminate in a cellular phenotype characterized by unregulated growth. Based on the knowledge, a variety of gene therapy strategies have been developed as potential new therapies for cancer. Current knowledge of proto­oncogene and tumor suppresser genes in the genesis of malignancy has stimulated the development of gene therapy tactics directed at ablating or restoring such genes, respectively. In other strategies, cancer cells are endowed with the ability to convert a systemically delivered prodrug to a toxic metabolite, or a target for destruction by replicating viral vectors conversely transfer of drug resistance genes into normal cells may provide chemoprotection during high dose antineoplastic treatment. Finally, immune system modulation can activate anticancer drug defense mechanisms [39] .

Oncogenes Inactivation

Several oncogenic proteins have been identified and associated with various malignancies. The most commonly applied approach in clinical trials to date has been use of antisense strategies. Transcription of oncogenes also can be inhibited by using adenoviral gene E1A, which interfere with the transcription of erbB-2, a strategy useful in treating cancer that over express this oncogenic protein, such as breast and ovarian cancer [39] .

Augmentation of Tumor Suppresser Genes

More then 24 tumor suppresser genes have been identified, and mutations in these genes have been associated with a variety of neoplastic conditions. Several clinical trials are under way to deliver p53 using adenoviral vectors to a variety of cancers. Similarly, viral vectors have been utilized to introduce a retinoblastoma gene and breast cancer gene BRCA1 into bladder and ovarian cancer, respectively. In some situations, this approach will fail, because the mutant gene exhibits dominant negative effects on the normal gene. To circumvent this problem for p53 gene therapy, a genetic repair strategy rather then a gene augmentation approach could be more effective.

Cell-Target Suicide

A conversion of a pro drug to a toxic metabolite by genetically engineering tumor cells is an attractive way to create an artificial difference between normal and neoplastic tissue. This can be achieved by the expression of a gene that confers a dominant, negatively selectable phenotype to the cancer cells, such as cell death imparted by expression of a prodrug - metabolism enzyme. Greater selectively in killing malignant cells will be obtained by transferring a gene that is not normally found inhuman beings (e.g. HSV-­thymidine kinase), rather then by overexpression an endogenous gene. The prototype for this approach utilizes the HSV-1 Thymidine kinase gene given to combination with produg ganciclovir in a manner distant from mammalian thymidine kinase. Phosphorylated ganciclovir is ultimately incorporated into DNA and inhibits DNA synthesis and transcription. The efficacy and safety on this approach is being tested in several clinical trials involving multiple malignancies [40] .

Chemoprotection Approach

The MDR-1 gene encoding the multidrug therapy transporter protein (also known as P- glycoprotein) has received much attention in this regard. This transmembrane protein transports a wide variety of chemotherapeutic agents (e.g. doxorubicin, vinaca alkaloids, epipodophyllotoxins and paclitaxel) and other drugs out of cells, thus protecting them from the agents' toxic effects.

Virus-mediated oncolysis

Certain viruses, including adenovirus, and HSV-1 can infect the lyse tumor cells. The use of oncolytic virus in combination with other gene based antineoplastic strategies has emerged as a promising addition to the multidimensional treatment cancers. Selective replication of virus in tumor cells leads to the cell lysis and to local dissemination of infective viral progeny to neighboring cancers cells. Most investigational uses of this strategy have utilized replication-competent adenovirus and HSV-1.


Various cytokines can enhance immunity against cancer cells, and this observation has stimulated the development of gene- based approaches to modulate the immune reaction in malignancy.

Ectopic Cytokine Expression: A variety of cytokine have been shown to decrease tumor growth when ectopically expressed in tumor cells or in there microenvironment. Some immunostimulatory agents do not alter the growth rate of the tumor initially, but lead to immunity against tumor growth if the animal is later challenged with wild type tumor cells.

Immune enhancement: One such approach is to express on the surface of cancer cells highly immunogenic molecule, such as allotype MHC antigens. It has been long known those additional "costimulatory' pathways distinct from the T-cell are needed to achieve T cell activation. The molecules B7-1 (CD 80) and B7-2 (CD 86) stimulate one such pathway. The B7s, whose expression normally is limited to antigen presenting cells and other specialized immune effector cells, engage specific receptors on the T cells surface in concert with antigen binding to the T-cell receptor [41] .

   Current Researches Top

Human Antimicrobial Protein hCAP18/LL-37 Promotes a Metastatic Phenotype in Breast Cancer

Human cathelicidin antimicrobial protein, hCAP18, and its C-terminal peptide LL-37 is a multifunctional protein. In addition to being important in antimicrobial defense, it induces chemotaxis, stimulates an giogenesis and promotes tissue repair. We previously showed that human breast cancer cells express high amounts of hCAP18, and hypothesised that hCAP18/LL-37 may be involved in tumor progression [42] .

Genetic variation in stromal proteins decorin and lumican with breast cancer: investigations in two case­control studies

The stroma is the supportive framework of biologic tissue in the breast, consisting of various proteins such as the proteoglycans, decorin and lumican. Altered expression of decorin and lumican is associated with breast tumors. We hypothesized that genetic variation in the decorin (DCN) and lumican (LUM) genes may contribute to breast cancer [43] .

Prognostic impact of tumor-specific HMG-CoA reductase expression in primary breast cancer

It has been previously reported that tumor-specific expression of the rate­limiting enzyme, 3-hydroxy-3­methylglutharyl-coenzyme A reductase (HMG-CoAR), in the mevalonate pathway is associated with more favorable tumor parameters in breast cancer. In the present study, it is examined the prognostic value of HMG­-CoAR expression in a large cohort of primary breast cancer patients with long-term follow up [44] .

Monoclonal antibodies in human cancer

Mouse, chimeric, humanized and human monoclonal antibodies (MABs) are all in use for treatment of human cancer. Antibodies can activate the immune system (antibody-dependent cellular cytotoxicity [ADCC], complement-dependent cytotoxicity [CDC], induction of tumor immunity [idiotype network]). The best therapeutic effect may be obtained if MABs are used early in the course of the disease [45] .

   Conclusion Top

The occurrence of breast cancer in female can be observed in only 5% cases with a malignant mass present with breast pain. Other symptoms such as immobility, skin changes (i. e, thickening, swelling, and redness) or nipple abnormalities (i.e., ulceration, retraction, spontaneous bloody discharge) may also be present at the same time. Today there are so many approaches, which can be made for the treatment of the cancer of breast such as surgery, radiation therapy chemotherapy, hormonal therapy and recently nanotechnology and gene therapy. With advances in screening, diagnosis, and treatment, the death rate for breast cancer has declined. In fact, about 90% of women newly diagnosed with breast cancer will survive for at least five years. Research is ongoing to develop even more effective screening and treatment programs.

   References Top

1.Cancer-Its various types along with causes, symptoms, treatments and stages, in: cancer info guide, 2009. http://www.cancer-info-guide.com/ (15 Mar. 2010).  Back to cited text no. 1
2.Mieszkowski, M. R., Cancer - A biophysicist′s point of view. In: Digital Recordings. 04 Sept. 2006. http://www.digital-recordings.com/publ/cancer.html (15 Mar 2010).  Back to cited text no. 2
3.Immune system. In: Kids Health. 2010. http://kidshealth.org/parent/general/body_basics/immune.html# (16 Mar. 2010).  Back to cited text no. 3
4.Helmberg, A, Carinogenesis. 2010. http://helmberg.at/carcinogenesis.htm (17 Mar. 2010).  Back to cited text no. 4
5.Diet and Physical Activity: What′s the Cancer Connection? In: Prevention & Early Detection. 22 Oct. 2009. http://www.cancer.org/docroot/PED/content/PED_3_1x_Link_Between_Lifestyle_and_CancerMarch03.asp (17 Mar. 2010).  Back to cited text no. 5
6.Margot. New SEER Report Documents High Risk of Second Cancers in Cancer Survivors. Oncology Times. 2007; 29(5): 8.  Back to cited text no. 6
7.Ershler W.B. The Influence of Advanced Age on Cancer Occurrence and Growth. In: Balducci L., Extermann M, editors. Biological Basis of Geriatric Oncology. Springer US; 2005; 124: 75-87.  Back to cited text no. 7
8.http://www.breastcancersource.com/?item1d=2784236 (17 Mar. 2010).  Back to cited text no. 8
9.Khuwaja G. A., Abu-Rezq A. N. Bimodal breast cancer classification system. Pattern Analysis and application, 2004; 7: 235-242.  Back to cited text no. 9
10.Breast cancer process india, Breast cancer cost india, Breast cancer, delhi India. Breast cancer information and resources. 13 April 2010. http://www.digforthecure. org/ breast-cancer-process-india-breast-cancer-cost-india-breast-cancer--delhi-india.html (14 April 2010).  Back to cited text no. 10
11.What is breast cancer? Imaginis. 11 Jun, 2008. http://www.imaginis.com/breast-health/what-is-breast-cancer-2 (17 Mar 2010).  Back to cited text no. 11
12.What is breast cancer? American cancer society. 18 Sept. 2009. http://www.cancer.org/docroot/CRI/content/CRI 2_4_1X_What is breast_cancer_5.asp (18 Mar 2010).  Back to cited text no. 12
13.Breast cancer. merck. 2008. http://www/merck.com/mmhe/sec22/ch251/ch251f.html (18 Mar. 2010).  Back to cited text no. 13
14.Types of breast cancer. Rethink breast cancer. 2003. http://www.rethinkbreastcancer.com/types_of_breast_cancer. html (18 Mar. 2010).  Back to cited text no. 14
15.Types of breast cancer. Abviva. 2009. http://abviva.com/1.html (18 Mar. 2010).  Back to cited text no. 15
16.Ductal breast cancer. Cancer studies. 24 Mar. http://cancer-studies.com/ductal-breast-cancer (28 Mar. 2010).  Back to cited text no. 16
17.Rayed L. Types of breast cancer. About.com: Cancer. 09 Jul. 2009. http://cancer.about.com/od/breastcancer/a/cancertypes. htm (20 Mar. 2010).  Back to cited text no. 17
18.Stephan P. Mucinous (Colloid) Carcinoma of the breast. About.com: Cancer. 05 Aug. 2008. http://breastcancer.about.com/od/types/p/mucinous_ca.htm (20 Mar. 2010).  Back to cited text no. 18
19.Hartmann L. C., Sellers T. A., Frost M. H. Lingle W. L., Degnim A. C., Ghosh K., Vierkant R. A., Maloney S. D., Pankratz V. S., Hillman D. W., Suman V. J., Blake C., Tlsty T., Vachon C. M.. Benign breast disease and the risk of breast cancer. N Engl J Med. 2005; 353; 229-237.  Back to cited text no. 19
20.Eberl M. M., Sunga A. Y., Farrell C. D., Mahoney M. C. Patients with a Family History of Cancer: Identification and Management. JABFM. 2005; 18: 211-217.  Back to cited text no. 20
21.Breast cancer. emedicinehealth. 2010. http://www.emedicinehealth.com/breast_cancer/page2_em. htm (20 Mar 2010).  Back to cited text no. 21
22.Fletcher S. W. Patient information: Risk factor for breast cancer. Up-To--Date. 29 Jan 2008. http://www.utdol.coin/patients/content/topic.do?topicKey=~_rZvVFHbE jbw (20 Mar 2010).  Back to cited text no. 22
23.Tiernan A. M. Behavioral risk factor in breast cancer: Can risk be modified? The Oncologist. 2003; 8: 326-334.  Back to cited text no. 23
24.Definite breast cancer risks.CancerHelp UK. 26 Sept 2008. http://www.cancerhelp.org.uk/type/breast--cancer/about/risks/definite-breast--cancer-risks (20 Mar 2010).  Back to cited text no. 24
25.Stephan P., What you need to know about breast cancer symptoms. About.com: Breast cancer. 06 Dec 2007). http://breastcancer.about.corn/od/whatisbreastcancer/a/bc_symptoms.htm (20 Mar 2010).  Back to cited text no. 25
26.Smith R. A. Cokkinides V., Brawley O. W. Cancer screening in the United States, 2008. CA Cancer J Clin, 2008; 58: 161-179.  Back to cited text no. 26
27.Lippman M. E., Breast cancer, Fauci A. S. editors. Harrison′s Principles of Internal Medicine. 17th ed. Library of Congress Cataloging in Publication Data; 2008.  Back to cited text no. 27
28.Stages of breast cancer, Breastcancer.org. 21 Jan 2010. http://www.breastcancer.org/symptoms/diagnosis/staging.jsp (20 Mar 2010).  Back to cited text no. 28
29.Breast cancer treatment, the breast cancerlnfo.com. http://thebreastcancerinfo.com/breast_cancer_treatment.htm (21 Mar 2010).  Back to cited text no. 29
30.Surgical oncology. UT health science center. 24 Sept 2009. http://www.surgery.uthscsa.edu/surgicaloncology/breast.asp (21 Mar 2010).  Back to cited text no. 30
31.Rath G. K. Radiation Therapy in the Management of Cancer. 50 Years of Cancer Control in India. http://mohfw.nic.in/pg96to104.pdf (21 Mar 2010).  Back to cited text no. 31
32.Detailed guide: Breast cancer radiation therapy. American cancer society. 18 Sept 2009. http://www.cancer.org/docroot/CRI/content/CRI_2_4_4X_Radiation_Therapy_5.asp?sitearea (21 Mar 2010).  Back to cited text no. 32
33.Breast health chemotherapy for breast cancer treatment; University Virginia Health System. 29 Aug 2006. http://www.health system.virginia.edu/uvahealth/adult_breast/chemo.cfm (21 Mar 2010).  Back to cited text no. 33
34.Cancer.Wellness.com.2006-2010. http://www.wellness.com/reference/conditions/cancer/prevention-and--treatment (21 Mar 2010).  Back to cited text no. 34
35.Wells B G. Breast Cancer, Pharmacotherapy hand book. 5th ed. New Delhi, Tata McGraw hill publishing company limited; 2004.  Back to cited text no. 35
36.Tanaka T., Decuzzi P., Cristofanilli M., Sakamoto J. M., Tasciotti V., Robertson F. M., Ferrari M. Nanotechnology for breast cancer therapy. Biomed Microdevices, 2009; 11: 49-63.  Back to cited text no. 36
37.McGu ire W. L. Steroid receptors in human breast cancer. Cancer research. 1978; 38: 4289-4291.  Back to cited text no. 37
38.Clark G. M., McGuire W. L. Progesterone receptors and human breast cancer. Breast cancer research and treatment. 1983; 3: 157-163.  Back to cited text no. 38
39.Osborne C., Wilson P., Tripathy D. Oncogenes and tumor suppresser genes in breast cancer. Potential diagnostic and therapeutic applications. The oncologist. 2004; 9: 361-377.  Back to cited text no. 39
40.Jin-Hui W., Xin-Yuan L. Targeting Strategies in Cancer Gene Therapy. ACTH Biochimica and biophysics sinica. 2003; 35: 311-316.  Back to cited text no. 40
41.Disis M. L., Park K. H., Immunomodulation of breast cancer via tumor antigen specific Th1. Cancer res treat. 2009; 41: 117-121.  Back to cited text no. 41
42.Weber G., Chamorro C. I., Granath F., Liljegren A., Zreika S., Saidak Z., Sandstedt B., Rotstein S., Mentaverri R., Sanchez F., Pivarcsi A., Stahle M.. Human antimicrobial protein hCAP18/LL-37 promotes a metastatic phenotype in breast cancer. Breast cancer research. 2009; 11: R6.  Back to cited text no. 42
43.Kelemen L. E., Couch F. J., Ahmed S., Dunning A. M., Pharoah P. D., Easton D. F., Fredericksen Z. S., Vierkant R. A., Pankratz V. S., Goode E. L., Scott C. G., Rider D. N., Vachon C. M.. Genetic variation in stromal proteins decorin and lumican with breast cancer: investigations in two case-control studies. Breast cancer research. 2008; 10: R98.  Back to cited text no. 43
44.Borggist S., Jogi A., Ponten F., Ryden L., Brennan D. J., Jirstrom K.. Prognostic impact of tumor-specific HMG-CoA reductase expression in primary breast cancer. Breast cancer research. 2008; 10:R79.  Back to cited text no. 44
45.Mellstedt H. Monoclonal antibody in human cancer. Medicamentos de actualidad. 2003;39:1-16.  Back to cited text no. 45


  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]

  [Table 1], [Table 2], [Table 3]

This article has been cited by
Rupani AR, Bhattacharjee B
International Journal of Pharmaceutical Sciences and Research. 2011; 2(1): 153-159


    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

  In this article
    Breast Cancer
    Types of Breast ...
    Causes of Breast...
    Current Researches
    Article Figures
    Article Tables

 Article Access Statistics
    PDF Downloaded2415    
    Comments [Add]    
    Cited by others 1    

Recommend this journal